The Food & Drug Administration released a list of pre-market approvals granted in March:
PMA Original Approvals
| APPLICATION NUMBER / DATE of APPROVAL | DEVICE TRADE NAME | COMPANY NAME CITY, STATE, & ZIP | DEVICE DESCRIPTION / INDICATIONS |
|---|---|---|---|
| P080020
3/22/11 |
Gel-One | Seikagaku Corporation
Tokyo, Japan 100-0005 |
Approval for the Gel-One™. The device is indicated for the treatment of pain in osteoarthritis (OA) of the knee in patients who have failed to respond adequately to non-pharmacologic therapy, non-steroidal anti-inflammatory drugs (NSAIDs) or analgesics, e.g., acetaminophen. |
| P080025
3/14/11 |
Medtronic® InterStim® Therapy System | Medtronic Neuromodulation
Minneapolis, MN 55432 |
Approval for the Medtronic® InterStim® Therapy System. The device is indicated for the treatment of chronic fecal incontinence in patients who have failed or could not tolerate more conservative treatments. |
PMA Supplemental Approvals
| APPLICATION NUMBER / DATE of APPROVAL | DEVICE TRADE NAME | COMPANY NAME CITY, STATE, & ZIP | DEVICE DESCRIPTION / INDICATIONS |
|---|---|---|---|
| N18033/S048
3/10/11 135-Day |
VISTAKON (etafilconA) Contact Lens | Johnson & Johnson Vision Care, Inc.
Jacksonville, FL 32256 |
Approval to implement an alternate method for re-sampling lenses. |
| P830055/S115
3/11/11 135-Day |
LCS Complete Total Knee System | DePuy Orthopaedics, Inc.
Warsaw, IN 46581 |
Approval for: 1) automating all milling/grinding processes that were previously manual; 2) use of an oil-based coolant during milling/ grinding; and 3) including a new process – manual in-process clean (IPC) to remove the oil-based coolant after milling. |
| P840001/S102
3/15/11 Real-Time |
Restore Implantable Neurostimulators | Medtronic Neurological
Minneapolis, MN 55432 |
Approval for minor firmware change. |
| P850007/S031
3/11/11 Real-Time |
Spinal-Stim | Orthofix, Inc.
Lewisville, TX 75056 |
Approval for design modifications to the garment covering, the treatment coils, liquid crystal display, control unit housing profile, orientation of the controls, software/ firmware, power supply cord, and labeling. The device, as modified, will be marketed under the trade name Spinal-Stim and is indicated as a spinal fusion adjunct to increase the probability of fusion success and as a non-operative treatment for salvage of failed spinal fusion, where a minimum of nine months has elapsed since the last surgery. |
| P860004/S138
3/3/11 135-Day |
SynchroMed II Infusion System | Medtronic Neuromodulation
Minneapolis, MN 55432 |
Approval of the following manufacturing process changes related to the Baseline test of the Implantable SynchroMed II Infusion Pump, Model 8637: 1) automation of the transfer of baseline test data; 2) change the duty cycle and lower the specification limit of the dynamic current test; and 3) an increase to the time to measure the micro awake current. |
| P860019/S264
3/31/11 135-Day |
Apex Monorail and Apex Over-the-Wire PTCA Dilation Catheter/Maverick 2 Monorail PTCA Catheter/Maverick Over-the-Wire PTCA Catheter/Maverick | Boston Scientific Corporation
Maple Grove, MN 55311 |
Approval for a change to the sterilization equipment. |
| P880006/S067
3/4/11 180-Day |
Merlin Patient Care System | St. Jude Medical
Sylmar, CA 91342 |
Approval for the Model 3330 Version 11.1 Software for the Model 3650 Merlin Patient Care System. |
| P880086/S189
3/4/11 180-Day |
Merlin Patient Care System | St. Jude Medical
Sylmar, CA 91342 |
Approval for the Model 3330 Version 11.1 Software for the Model 3650 Merlin Patient Care System. |
| P890003/S177
3/25/11 180-Day |
Carelink Monitor and CardioSight® Reader | Medtronic, Inc.
Mounds View, MN 55112 |
Approval for Protecta™ XT CRT-D D314TRG and Protecta™ CRT-D D334TRG Implantable Cardioverter Defibrillators with Cardiac Resynchronization, Protecta™ XT DR D314DRG, Protecta™ XT VR D314VRG, Protecta™ DR D334DRG, and Protecta™ VR D334VRG Implantable Cardioverter Defibrillators, Model SW009 Application Software v1.0, Carelink Monitor Model 2490C upgrade, CardioSight Reader Model 2020A upgrade, and Model 2491 DDMA upgrade. |
| P890003/S178
3/22/11 Real-Time |
Software Version SW003 (version 7.1); Relia Application Software Version SW010 (version 7.1); and Carelink DDMA Version K3 DDMA1 2v4 | Medtronic, Inc.
Mounds, View, MN 55112 |
Approval for nEw Application Software Version SW003 (version 7.1); Relia Application Software Version SW010 (version 7.1); and Carelink DDMA Version K3 DDMA1 2v4. |
| P890003/S189
3/22/11 180-Day |
Consulta CRT-P and Syncra CRT-P Implantable Pulse Generators with Cardiac Resynchronization, | Medtronic, Inc.
Mounds View, MN 55112 |
Approval for the Consulta CRT-P C4TR01 and Syncra CRT-P C2TR01 Implantable Pulse Generators with Cardiac Resynchronization, Software Model 9995 (version 7.3), CareLink Monitor Model 2490G and Model 2491 DDMA. |
| P890003/S192
3/22/11 180-Day |
Preva, Prevade and Prodigy IPGs | Medtronic, Inc.
Mounds, View, MN 55112 |
Approval for the change of the materials, power supply, and incoming inspection
process for the following AVX capacitors to be used in the above referenced IPGs. Those capacitors are: XT009, XT045, XT082, XT096, XT113, XTC002, XTC018, XTC029, XT014, XT053, XT084, XT097, XT114, XTC004, XTC019, XTC030, XT017, XT058, XT085, XT099, XT116, XTC005, XTC020, XT023, XT060, XT086, XT103, XT118, XTC006, XTC021, XT027, XT067, XT087, XT104, XT120, XTC007, XTC023, XT032, XT068, XT088, XT105, XT121, XTC008, XTC024, XT038, XT070, XT090, XT106, XT122, XTC009, XTC025, XT041, XT072, XT091, XT108, XT123, XTC010, XTC026, XT043, XT077, XT092, XT109, XT124, XTC013, XTC027, XT044, XT078, XT095, XT110, XTC001, XTC017, XTC028, XT097, XT118, XT009, XT017, XT044, XT070, XT085, XT087, and XT114. |
| P890003/S195
3/17/11 Real-Time |
CareLink Remote Home Monitor | Medtronic, Inc.
Mounds View, MN 55112 |
Approval to reduce the 21-day scheduling of device interrogation requirement within the device firmware, as well as labeling modifications to disclose the effects of this programmability on the longevity of the pulse generators. |
| P890003/S210
3/17/11 Real-Time |
CareLink Home Monitor, Device and Data Management Application and CardioSight Reader | Medtronic, Inc.
Mounds View, MN 55112 |
Approval for modifications to the CareLink Home Monitor Model 2490G, Device and Data Management Application Model 2491, and CardioSight Reader Model 2020A. |
| P890055/S028
3/15/11 180-Day |
MedStream Programmable Infusion System | Codman & Shurtleff, Inc.
Raynham, MA 02767 |
Approval of the post-approval study protocol. |
| P890055/S029
3/15/11 180-Day |
MedStream Programmable Infusion System | Codman & Shurtleff, Inc.
Raynham, MA 02767 |
Approval of the post-approval study protocol. |
| P890055/S030
3/15/11 180-Day |
MedStream Programmable Infusion System | Codman & Shurtleff, Inc.
Raynham, MA 02767 |
Approval of the post-approval study protocol. |
| P900056/S103
3/31/11 135-Day |
Rotablator Rotational Angioplasty System | Boston Scientific Corporation
Maple Grove, MN 55311 |
Approval for a change to the sterilization equipment. |
| P910007/S019
3/22/11 180-Day |
ARCHITECT Total PSA | Abbott Laboratories Abbott Park, IL 60064 | Approval for a manufacturing site located at Abbott Ireland Diagnostics Division in Sligo Ireland. |
| P910023/S236
3/4/11 180-Day |
Merlin Patient Care System | St. Jude Medical
Sylmar, CA 91342 |
Approval for the Model 3330 Version 11.1 Software for the Model 3650 Merlin Patient Care System. |
| P910077/S110
3/3/11 Real-Time |
Latitude Patient Management System | Guidant Corporation ( Boston Scientific Corporation)
St. Paul, MN 55112 |
Approval for modification to the
Latitude Patient Management System Regulated Application Software v7.0.02 on Latitude System Server (Model 6488) and Related Communicator Software Changes (Model 6476). |
| P920047/S044
3/31/11 135-Day |
Blazer II XP Cardiac Ablation Catheter/Cable/ Blazer II High Torque Distal (HTD) Ablation Catheter/Cable/ Blazer Prime | Boston Scientific Corporation
Maple Grove, MN 55311 |
Approval for a change to the sterilization equipment. |
| P930016/S034
3/4/11 180-Day |
STAR S4 IR Excimer Laser System with Variable Spot Scanning and WaveScan WaveFront System | AMO Manufacturing USA, LLC
Milpitas, CA 95035 |
Approval for WaveScan Wave- Front Software Version 3.68. |
| P950029/S056
3/22/11 Real-Time |
Reply/Esprit SR/DR Pacers | Ela Medical ,Inc. (Sorin Group)
Plymouth, MN 55441 |
Approval for a new Setscrew and Torque-limiting Screwdriver Accessory. |
| P950037/S091
3/25/11 180-Day |
Envia, Entovis, Estella, Ecuro and Effecta Family of Pulse Generators | Biotronik, Inc.
Lake Oswego, OR 97035 |
Approval for updated integrated circuits for use in the currently marketed Evia/ Entovis/Estella/ Ecuro/Effecta family of pulse generators. |
| P960011/S018
3/8/11 180-Day |
BVI 1% OVD Sodium Hyaluronate | Ferring Pharmaceuticals, Inc.
Parsippany, NJ 07054 |
Approval for 1) the inclusion of directions for proper finger flange orientation in the Instructions for Use, and approval to change the trade name of the device from BD 1% OVD Sodium Hyaluronate to BVI 1% OVD Sodium Hyaluronate. |
| P970012/S068
3/22/11 180-Day |
Kappa IPGs | Medtronic, Inc.
Mounds, View, MN 55112 |
Approval for the change of the materials, power supply, and incoming inspection
process for the following AVX capacitors to be used in the above referenced IPGs. Those capacitors are: XT009, XT045, XT082, XT096, XT113, XTC002, XTC018, XTC029, XT014, XT053, XT084, XT097, XT114, XTC004, XTC019, XTC030, XT017, XT058, XT085, XT099, XT116, XTC005, XTC020, XT023, XT060, XT086, XT103, XT118, XTC006, XTC021, XT027, XT067, XT087, XT104, XT120, XTC007, XTC023, XT032, XT068, XT088, XT105, XT121, XTC008, XTC024, XT038, XT070, XT090, XT106, XT122, XTC009, XTC025, XT041, XT072, XT091, XT108, XT123, XTC010, XTC026, XT043, XT077, XT092, XT109, XT124, XTC013, XTC027, XT044, XT078, XT095, XT110, XTC001, XTC017, XTC028, XT097, XT118, XT009, XT017, XT044, XT070, XT085, XT087, and XT114. |
| P970013/S034
3/4/11 180-Day |
Merlin Patient Care System | St. Jude Medical
Sylmar, CA 91342 |
Approval for the Model 3330 Version 11.1 Software for the Model 3650 Merlin Patient Care System. |
| P980003/S024
3/31/11 135-Day |
Chilli II Cooled Ablation Catheter and Cable | Boston Scientific Corporation
Maple Grove, MN 55311 |
Approval for a change to the sterilization equipment. |
| P980007/S011
3/31/11 180-Day |
Abbott Architect Free PSA | Abbott Laboratories
Abbott Park, IL 60064 |
Approval for a manufacturing site located at Abbott Ireland Diagnostics Division in Sligo, Ireland. |
| P980016/S211
3/25/11 180-Day |
Protecta™ XT DR, Protecta™ XT VR, Protecta™ DR, and Protecta™ VR, Implantable Cardioverter Defibrillators;
Model SW009 Application Software vi.0 Systems
|
Medtronic, Inc.
Mounds View, MN 55112 |
Approval for Protecta™ XT CRT-D D314TRG and Protecta™ CRT-D D334TRG Implantable Cardioverter Defibrillators with Cardiac Resynchronization, Protecta™ XT DR D314DRG, Protecta™ XT VR D314VRG, Protecta™ DR D334DRG, and Protecta™ VR D334VRG Implantable Cardioverter Defibrillators, Model SW009 Application Software v1.0, Carelink Monitor Model 2490C upgrade, CardioSight Reader Model 2020A upgrade, and Model 2491 DDMA upgrade. |
| P980016/S240
3/22/11 180-Day |
Marquis DR/VR; Maximo DR/VR; Intrinsic 30 /Intrinsic; EnTrust; Maximo II; Virtuoso DR; Virtuoso II; Secura | Medtronic, Inc.
Mounds, View, MN 55112 |
Approval for the change of the materials, power supply, and incoming inspection
process for the following AVX capacitors to be used in the above referenced IPGs. Those capacitors are: XT009, XT045, XT082, XT096, XT113, XTC002, XTC018, XTC029, XT014, XT053, XT084, XT097, XT114, XTC004, XTC019, XTC030, XT017, XT058, XT085, XT099, XT116, XTC005, XTC020, XT023, XT060, XT086, XT103, XT118, XTC006, XTC021, XT027, XT067, XT087, XT104, XT120, XTC007, XTC023, XT032, XT068, XT088, XT105, XT121, XTC008, XTC024, XT038, XT070, XT090, XT106, XT122, XTC009, XTC025, XT041, XT072, XT091, XT108, XT123, XTC010, XTC026, XT043, XT077, XT092, XT109, XT124, XTC013, XTC027, XT044, XT078, XT095, XT110, XTC001, XTC017, XTC028, XT097, XT118, XT009, XT017, XT044, XT070, XT085, XT087, and XT114. |
| P980016/S268
3/22/11 Real-Time |
Maximo II, Secura, and Virtuoso II | Medtronic, Inc.
Mounds View, MN 55112 |
Approval for the design changes to the Multilayer Ceramic Capacitors (XC308, XC251, XC259, and XC263) for Concerto II Model D274TRK; Consulta Model D224TRK; and Maximo II Model
D284TRK; Maximo II Models D284DRG, D2S4VRC; Secura Models D224DRG, D224VRC; and Virtuoso Models D274DRG. D274VRG; EnRhythm Model P1501DR; Vitatron DA+ C- Series Models C20A1, C20A3, C60A1, C60A3; and Vitatron DA+ T-Series Models T2OA1, T6OA1; |
| P980035/S147
3/22/11 Real-Time |
nEw Application Software Version SW003 (version 7.1); Relia Application Software Version SW010 (version 7.1); and Carelink DDMA Version K3 DDMA1 2v4 | Medtronic, Inc.
Mounds, View, MN 55112 |
Approval for nEw Application Software Version SW003 (version 7.1); Relia Application Software Version SW010 (version 7.1); and Carelink DDMA Version K3 DDMA1 2v4. |
| P980035/S168
3/22/11 180-Day |
Adapta; Relia; Sensia; Versa; Kappa; EnPulse; Sigma | Medtronic, Inc.
Mounds, View, MN 55112 |
Approval for the change of the materials, power supply, and incoming inspection
process for the following AVX capacitors to be used in the above referenced IPGs. Those capacitors are: XT009, XT045, XT082, XT096, XT113, XTC002, XTC018, XTC029, XT014, XT053, XT084, XT097, XT114, XTC004, XTC019, XTC030, XT017, XT058, XT085, XT099, XT116, XTC005, XTC020, XT023, XT060, XT086, XT103, XT118, XTC006, XTC021, XT027, XT067, XT087, XT104, XT120, XTC007, XTC023, XT032, XT068, XT088, XT105, XT121, XTC008, XTC024, XT038, XT070, XT090, XT106, XT122, XTC009, XTC025, XT041, XT072, XT091, XT108, XT123, XTC010, XTC026, XT043, XT077, XT092, XT109, XT124, XTC013, XTC027, XT044, XT078, XT095, XT110, XTC001, XTC017, XTC028, XT097, XT118, XT009, XT017, XT044, XT070, XT085, XT087, and XT114. |
| P980035/S197
3/22/11 Real-Time |
EnRhythm | Medtronic, Inc.
Mounds View, MN 55112 |
Approval for the design changes to the Multilayer Ceramic Capacitors (XC308, XC251, XC259, and XC263) for Concerto II Model D274TRK; Consulta Model D224TRK; and Maximo II Model
D284TRK; Maximo II Models D284DRG, D2S4VRC; Secura Models D224DRG, D224VRC; and Virtuoso Models D274DRG. D274VRG; EnRhythm Model P1501DR; Vitatron DA+ C- Series Models C20A1, C20A3, C60A1, C60A3; and Vitatron DA+ T-Series Models T2OA1, T6OA1; |
| P980037/S034
3/17/11 Real-Time |
AngioJet® Rheolytic™ Thrombectomy System | Medrad Interventional/ Possis
Minneapolis, MN 55433 |
Approval for changes to the AngioJet Ultra Console software. |
| P990001/S068
3/22/11 180-Day |
Vitatron DA+ C Series and T Series IPGs; Jade II, Topaz II, Vita IPGs | Medtronic, Inc.
Mounds, View, MN 55112 |
Approval for the change of the materials, power supply, and incoming inspection
process for the following AVX capacitors to be used in the above referenced IPGs. Those capacitors are: XT009, XT045, XT082, XT096, XT113, XTC002, XTC018, XTC029, XT014, XT053, XT084, XT097, XT114, XTC004, XTC019, XTC030, XT017, XT058, XT085, XT099, XT116, XTC005, XTC020, XT023, XT060, XT086, XT103, XT118, XTC006, XTC021, XT027, XT067, XT087, XT104, XT120, XTC007, XTC023, XT032, XT068, XT088, XT105, XT121, XTC008, XTC024, XT038, XT070, XT090, XT106, XT122, XTC009, XTC025, XT041, XT072, XT091, XT108, XT123, XTC010, XTC026, XT043, XT077, XT092, XT109, XT124, XTC013, XTC027, XT044, XT078, XT095, XT110, XTC001, XTC017, XTC028, XT097, XT118, XT009, XT017, XT044, XT070, XT085, XT087, and XT114. |
| P990001/S080
3/22/11 Real-Time |
Vitatron DA+ C-Series; and Vitatron DA+T-Series | Medtronic, Inc.
Mounds View, MN 55112 |
Approval for the design changes to the Multilayer Ceramic Capacitors (XC308, XC251, XC259, and XC263) for Concerto II Model D274TRK; Consulta Model D224TRK; and Maximo II Model
D284TRK; Maximo II Models D284DRG, D2S4VRC; Secura Models D224DRG, D224VRC; and Virtuoso Models D274DRG. D274VRG; EnRhythm Model P1501DR; Vitatron DA+ C- Series Models C20A1, C20A3, C60A1, C60A3; and Vitatron DA+ T-Series Models T2OA1, T6OA1; |
| P000021/S018
3/11/11 180-Day |
Dimension® FPSA Flex® Reagent Cartridge | Siemens Healthcare Diagnostics, Inc.
Newark, DE 19714 |
Approval for software changes (Version 3.1.1. to 3.3.) and associated hardware changes to the Dimension Vista® System. |
| P010013/S031
3/9/11 135-Day |
NovaSure Impedance Controlled Endometrial Ablation System | Hologic, Inc.
Marlborough, MA 01752 |
Approval for an annealing process to the molded front grip component. |
| P010015/S084
3/22/11 180-Day |
Consulta CRT-P and Syncra CRT-P Implantable Pulse Generators with Cardiac Resynchronization, Software Model 9995 (version 7.3), CareLink Monitors | Medtronic, Inc.
Mounds View, MN 55112 |
Approval for the Consulta CRT-P C4TR01 and Syncra CRT-P C2TR01 Implantable Pulse Generators with Cardiac Resynchronization, Software Model 9995 (version 7.3), CareLink Monitor Models 2490G and Model 2491 DDMA. |
| P010015/S086
3/22/11 180-Day |
InSync/InSync III CRT-Ps | Medtronic, Inc.
Mounds, View, MN 55112 |
Approval for the change of the materials, power supply, and incoming inspection
process for the following AVX capacitors to be used in the above referenced IPGs. Those capacitors are: XT009, XT045, XT082, XT096, XT113, XTC002, XTC018, XTC029, XT014, XT053, XT084, XT097, XT114, XTC004, XTC019, XTC030, XT017, XT058, XT085, XT099, XT116, XTC005, XTC020, XT023, XT060, XT086, XT103, XT118, XTC006, XTC021, XT027, XT067, XT087, XT104, XT120, XTC007, XTC023, XT032, XT068, XT088, XT105, XT121, XTC008, XTC024, XT038, XT070, XT090, XT106, XT122, XTC009, XTC025, XT041, XT072, XT091, XT108, XT123, XTC010, XTC026, XT043, XT077, XT092, XT109, XT124, XTC013, XTC027, XT044, XT078, XT095, XT110, XTC001, XTC017, XTC028, XT097, XT118, XT009, XT017, XT044, XT070, XT085, XT087, and XT114. |
| P010031/S171
3/25/11 180-Day |
Protecta™ XT CRT-D and Protecta™ CRT-D Implantable Cardioverter Defibrillators with Cardiac Resynchronization; Model SW009 Application Software vi.0 Systems | Medtronic, Inc.
Mounds View, MN 55112 |
Approval for Protecta™ XT CRT-D D314TRG and Protecta™ CRT-D D334TRG Implantable Cardioverter Defibrillators with Cardiac Resynchronization, Protecta™ XT DR D314DRG, Protecta™ XT VR D314VRG, Protecta™ DR D334DRG, and Protecta™ VR D334VRG Implantable Cardioverter Defibrillators, Model SW009 Application Software v1.0, Carelink Monitor Model 2490C upgrade, CardioSight Reader Model 2020A upgrade, and Model 2491 DDMA upgrade. |
| P010031/S198
3/22/11 180-Day |
InSync II Marquis; InSync III Marquis; InSync Sentry; InSync Maximo; Concerto; Concerto II; Consulta; Maximo II | Medtronic, Inc.
Mounds, View, MN 55112 |
Approval for the change of the materials, power supply, and incoming inspection
process for the following AVX capacitors to be used in the above referenced IPGs. Those capacitors are: XT009, XT045, XT082, XT096, XT113, XTC002, XTC018, XTC029, XT014, XT053, XT084, XT097, XT114, XTC004, XTC019, XTC030, XT017, XT058, XT085, XT099, XT116, XTC005, XTC020, XT023, XT060, XT086, XT103, XT118, XTC006, XTC021, XT027, XT067, XT087, XT104, XT120, XTC007, XTC023, XT032, XT068, XT088, XT105, XT121, XTC008, XTC024, XT038, XT070, XT090, XT106, XT122, XTC009, XTC025, XT041, XT072, XT091, XT108, XT123, XTC010, XTC026, XT043, XT077, XT092, XT109, XT124, XTC013, XTC027, XT044, XT078, XT095, XT110, XTC001, XTC017, XTC028, XT097, XT118, XT009, XT017, XT044, XT070, XT085, XT087, and XT114. |
| P010031/S222
3/22/11 Real-Time |
Concerto II, Consulta, and Maximo II | Medtronic, Inc.
Mounds View, MN 55112 |
Approval for the design changes to the Multilayer Ceramic Capacitors (XC308, XC251, XC259, and XC263) for Concerto II Model D274TRK; Consulta Model D224TRK; and Maximo II Model
D284TRK; Maximo II Models D284DRG, D2S4VRC; Secura Models D224DRG, D224VRC; and Virtuoso Models D274DRG. D274VRG; EnRhythm Model P1501DR; Vitatron DA+ C- Series Models C20A1, C20A3, C60A1, C60A3; and Vitatron DA+ T-Series Models T2OA1, T6OA1; |
| P020009/S066
3/31/11 135-Day |
Express 2 Monorail and Over-the-Wire | Boston Scientific Corporation
Maple Grove, MN 55311 |
Approval for a change to the sterilization equipment. |
| P020025/S025
3/31/11 135-Day |
Blazer II XP Cardiac Ablation Catheter and Cable/Blazer Prime XP Cardiac Ablation | Boston Scientific Corporation
Maple Grove, MN 55311 |
Approval for a change to the sterilization equipment. |
| P020026/S081
3/3/11 135-Day |
CYPHER® Sirolimus-Eluting Coronary Stent, Coronary Stent on RAPTOR™ Over-the-Wire Delivery System/
RAPTORRAIL® Rapid Exchange Delivery System (Cypher Stent®) |
Cordis Corporation Miami Lakes, FL
33014 |
Approval for automation of your stent coating process. |
| P020027/S013
3/11/11 180-Day |
Dimension® FPSA Flex® Reagent Cartridge | Siemens Healthcare Diagnostics, Inc. Newark, DE
19714 |
Approval for software changes (Version 3.1.1 to 3.3) and associated hardware changes to the Dimension Vista® System. |
| P030019/S017
3/18/11 135-Day |
Orthovisc® | Anika Therapeutics, Inc.
Bedford, MA 01730 |
Approval for the sample preparation of raw material hyaluronate acid to be changed from its current formulation to a more diluted test sample. |
| P030025/S091
3/31/11 135-Day |
Taxus Express 2 Paclitaxel-Eluting Coronary Stent System | Boston Scientific Corporation
Maple Grove, MN 55311 |
Approval for a change to the sterilization equipment. |
| P030031/S023
3/3/11 135-Day |
NaviStar® Thermocool® Diagnostic/Ablation Deflectable Tip Catheter | Biosense Webster, Inc.
Diamond Bar, CA 91765 |
Approval for addition of a label during a manufacturing process step. |
| P030034/S005
3/11/11 Real-Time |
Cervical-Stim | Orthofix, Inc.
Lewisville, TX 75056 |
Approval for design modifications to the garment covering, the treatment coils, liquid crystal display, control unit housing profile, orientation of the controls, software/ firmware, power supply cord, and labeling. The device, as modified, will be marketed under the trade name Cervical-Stim and is indicated as an adjunct to cervical fusion surgery in patients at high risk for non-fushion. |
| P030035/S070
3/4/11 180-Day |
Merlin Patient Care System | St. Jude Medical
Sylmar, CA 91342 |
Approval for the Model 3330 Version 11.1 Software for the Model 3650 Merlin Patient Care System. |
| P030036/S004
3/30/11 180-Day |
SelectSecure Lead | Medtronic, Inc.
Mounds View, MN 55112 |
Approval for improvements to the chemistry, manufacturing, and controls (CMC) and elution methods and specifications for the drug coating on SelectSecure Model 3830 leads. |
| P030052/S004
3/22/11 Special |
UroVysion Bladder Cancer Kit | Abbott Molecular, Inc.
Des Plaines, IL 60018 |
Approval to provide the definition for the pepsin activity of the Vysis protease reagent in the UroVysion package insert. |
| P030053/S011
3/17/11 180-Day |
MemoryGel™ Silicone-filled Breast implant | Mentor Corporation
Santa Barbara, CA 93111 |
Approval of the post-approval study protocol. |
| P030054/S153
3/4/11 180-Day |
Merlin Patient Care System | St. Jude Medical
Sylmar, CA 91342 |
Approval for the Model 3330 Version 11.1 Software for the Model 3650 Merlin Patient Care System. |
| P040016/S063
3/31/11 135-Day |
Veriflex (Liberté) Coronary Stent System | Boston Scientific Corporation
Maple Grove, MN 55311 |
Approval for a change to the sterilization equipment. |
| P040033/S020
3/16/11 Special |
Birmingham Hip Resurfacing (BHR) System | Smith & Nephew Orthopaedics
Cordova, TN 38016 |
Approval for revisions to the surgical technique manual. |
| P040036/S016
3/3/11 135-Day |
NaviStar® Thermocool® Diagnostic/Ablation Deflectable Tip Catheter | Biosense Webster, Inc.
Diamond Bar, CA 91765 |
Approval for addition of a label during a manufacturing process step. |
| P050007/S028
3/24/11 Special |
Starclose SE Vascular Closure
System |
Abbott Vascular Devices
Redwood City, CA 94063 |
Approval to add adjunctive compression language to the labeling and instructions for use. |
| P050010/S010
3/3/11 135-Day |
ProDisc™-L Total Disc Replacement | Synthes Spine
West Chester, PA 19380 |
Approval for a change from a manual deburring process to an automated brush deburring process. |
| P050018/S012
3/30/11 180-Day |
AngioSculpt® PTCA Scoring Balloon Catheter | AngioScore
Fremont, CA 94538 |
Approval for a manufacturing site located at Sterigenics in Salt Lake City, Utah. |
| P050039/S005
3/31/11 Special |
Exactech® Novation™ Ceramic AHS® Articulation Hip System | Exactech, Inc.
Gainesville, FL 32653 |
Approval for labeling changes which add strengthening language to the femoral stem surgical technique manuals. |
| P050042/S010
3/22/11 180-Day |
ARCHITECT Anti-HCV | Abbott Laboratories Abbott Park, IL 60064 | Approval for a manufacturing site located at Abbott Ireland Diagnostics Division in Sligo, Ireland. |
| P050043/S004
3/17/11 Real-Time |
Femoral Introducer Sheath and Hemostatic Device (FISH), FISH-SP Device | Morris Innovative Bloomington, IN
47403
|
Approval for: 1) replacing the sewn two-piece small intestine submocosa (SIS) assembly with a single SIS piece; 2) decreasing the SIS cuff length and ribbon width; 3) modifying the SIS patch to release wire connection; and 4) changing the sheath material from a high density polyethylene (HDPE) to fluorinated ethylene propylene (FEP). |
| P050047/S015
3/25/11 Special |
Juvéderm Hyaluronate Gel Implants | Allergan Medical Goleta, CA
93117 |
Approval for some labeling updates to improve the safe use of the device. |
| P050051/S009
3/22/11 180-Day |
ARCHITECT AUSAB | Abbott Laboratories Abbott Park, IL 60064 | Approval for a manufacturing site located at Abbott Ireland Diagnostics Division in Sligo, Ireland. |
| P060001/S011
3/8/11 180-Day |
Protégé GPS and Protégé RX Carotid Stent Systems | eV3, Inc.
Plymouth, MN 55441 |
Approval of the post-approval study protocol. |
| P060004/S001
3/28/11 Panel-Track |
MEL 80™ Excimer Laser System | Carl Zeiss Meditec, Inc.
Dublin, CA 94568 |
Approval for the MEL 80™ Excimer Laser System. This device uses an optical zone of 6.0 to 6.5 mm in diameter and a transition zone of 2.0 to 4.0 mm for a total ablation diameter of 10.0 mm, and is indicated for primary Laser Assisted in situ Keratomileusis (LASIK) treatments for: 1) the reduction or elimination of naturally-occurring hyperopia of less than or equal to
+5.0 D with or without refractive astigmatism of > +0.5 and ≤ +3.0D, with a maximum MRSE of +5.0D; 2) in patients who are 21 years of age or older; and 3) with documentation of stable manifest refraction over the past year as demonstrated by change in sphere and cylinder of ≤ 0.5D. |
| P060006/S017
3/31/11 135-Day |
Express SD Monorail Premounted Stent System | Boston Scientific Corporation
Maple Grove, MN 55311 |
Approval for a change to the sterilization equipment. |
| P060007/S007
3/22/11 180-Day |
ARCHITECT HBsAg/ Confirmatory | Abbott Laboratories Abbott Park, IL 60064 | Approval for a manufacturing site located at Abbott Ireland Diagnostics Division in Sligo, Ireland. |
| P060008/S057
3/1/11 180-Day |
TAXUS® Liberté® Paclitaxel-Eluting Coronary Stent System | Boston Scientific Corporation
Maple Grove, MN 55311 |
Approval for updating the Patient Guide into two separate documents (Angioplasty and Stent Education Guide and Patient Information Guide). |
| P060008/S060
3/31/11 135-Day |
Taxus Liberté Paclitaxel-Eluting Coronary Stent System | Boston Scientific Corporation
Maple Grove, MN 55311 |
Approval for a change to the sterilization equipment. |
| P060008/S068
3/11/11 180-Day |
TAXUS Liberté® | Boston Scientific Corporation
Maple Grove, MN 55311 |
Approval of the post-approval study protocol. |
| P060018/S002
3/24/11 135-Day |
PRESTIGE® Cervical Disc | Medtronic Sofamor Danek
Memphis, TN 38132 |
Approval for a change of location of the Orchid Anzon (formerly Anzon Company, Inc.) facility. |
| P060035/S006
3/22/11 180-Day |
ARCHITECT CORE-M | Abbott Laboratories Abbott Park, IL 60064 | Approval for a manufacturing site located at Abbott Ireland Diagnostics Division in Sligo, Ireland. |
| P070009/S012
3/31/11 135-Day |
REALIZE Adjustable Gastric Band with Injection Port and Applier | Ethicon Endo-Surgery, Inc.
Cincinnati, Oh 45242 |
Approval for the use of an alternate supplier for the injection molding of the septum and connector sleeve components of the injection port. |
| P070009/S013
3/31/11 Real-Time |
REALIZE® Adjustable Gastric Band with Injection Ports & Applier and REALIZE® Adjustable Gastric Band-C with Injection Ports & Applier and Injection Port | Ethicon Endo-Surgery, Inc.
Cincinnati, OH 45242 |
Approval for a device change to modify the silicone material used for the Injection Port septum and Injection Port connector sleeve components, along with a minor associated labeling modification. |
| P070014/S020
3/17/11 180-Day |
LifeStent Vascular Stent Systems | Bard Peripheral Vascular, Inc.
Tempe, AZ 85280 |
Approval of the post-approval study protocol. |
| P080006/S004
3/31/11 180-Day |
Attain Ability Straight Left Ventricular Lead | Medtronic, Inc.
Mounds View, MN 55112 |
Approval for the Attain Ability Straight Model 4396 Left Ventricular Lead. The Model 4396 lead is a 4 French, transvenous, steroid eluting, dual electrode, polyurethane insulated, single coil, straight tip, tine fixation lead intended for use in left heart coronary veins. |
| P080011/S004
3/23/11 180-Day |
Biofinity Contact Lenses | CooperVision, Inc. Pleasanton, CA
94588 |
Approval for an alternate labeling and packing site located at Cooper- Vision Inc., West Henrietta, New York. |
| P080014/S005
3/29/11 Real-Time |
CERVISTA HPV HR | Hologic, Inc.
Marlborough, MA 01752 |
Approval for the increase of the volume of the HPV control in Cervista HPV HR test and labeling changes to the package insert. |
| P080015/S002
3/29/11 Real-Time
|
CERVISTA HPV 16/18 | Hologic, Inc. Marlborough, MA 01752 | Approval for the increase of the volume of the HPV control in Cervista HPB 16/18 test and labeling changes to the package insert. |
| P080023/S006
3/22/11 180-Day |
ARCHITECT CORE | Abbott Laboratories Abbott Park, IL 60064 | Approval for a manufacturing site located at Abbott Ireland Diagnostics Division in Sligo, Ireland. |
| P080029/S001
3/11/11 180-Day |
Quick-Close® Vascular Suturing System | Interventional Therapies, LLC
North Attleboro, MA 02760 |
Approval for ergonomic changes to the Quick-Close® Vascular Suturing System. |
| P100010/S005
3/24/11 Real-Time |
Arctic Front® Cardiac CryoAblation Catheter | Medtronic CryoCath LP
Quebec, Canada H9R 5Z8 |
Approval for a labeling change to extend the shelf-life of the device. |
30-Day Notices (135 Day Supplement was not required)
| APPLICATION NUMBER / DATE of APPROVAL | DEVICE TRADE NAME | COMPANY NAME CITY, STATE, & ZIP | DEVICE DESCRIPTION / INDICATIONS |
|---|---|---|---|
| N12159/S027
3/4/11 |
Surgicel Original, Surgicel Fibrillar and Surgicel
NU-KNIT Absorbable Hemostats |
Ethicon Incorporated
Somerville, NJ 08876 |
Alternate cycle for the dehumidification oven. |
| N16895/S093
3/4/11 |
Bausch & Lomb SofLens (polymacon) Visibility Tinted Contact Lenses | Bausch & Lomb, Incorporated
3/4/11 |
Change to transfer raw material supplier processing from Sarasota, Florida to Germany. |
| P830061/S060
3/30/11 |
CapSure, Vitatron, Crystaline, Vitatron Excellence PS+ | Medtronic, Inc.
Mounds View, MN 55112 |
Update to the sterile packaging operation process. |
| P840001/S179
3/9/11 |
Restore Implantable Neurostimulators | Medtronic, Inc.
Minneapolis, MN 55432 |
Implementation of an additional automated plating line at the plating supplier. |
| P840001/S180
3/9/11 |
Itrel®, Synergy® and Synergy Versitrel® IPGs, RestorePrime®, PrimeAdvanced®, Restore®, RestoreUltra® and RestoreAdvanced® INS | Medtronic, Inc.
Minneapolis, MN 55432 |
Modification to epoxy dispense equipment parameters. |
| P840001/S181
3/17/11 |
Itrel 3 INS, Synergy Family INS, Pocket Adaptors | Medtronic Neuromodulation
Minneapolis, MN 55432 |
Addition of a new manufacturing mold and component supplier. |
| P850079/S049
3/16/11 |
Frequency XCEL Toric (Methafilcon a) Soft Contact Lens | CooperVision, Inc.
Pleasanton, CA 94588 |
Change in location of the wet processing area and the use of an alternate biological indicator for sterilization release. |
| P850089/S073
3/30/11 |
Capsure, Z Novus, Vitatron, Excellence SS+, Impulse II | Medtronic, Inc.
Mounds View, MN 55112 |
Update to the sterile packaging operation process. |
| P860004/S146
3/9/11 |
SynchroMed II Implantable Drug Pump | Medtronic, Inc.
Minneapolis, MN 55432 |
Implementation of an additional automated plating line at the plating supplier. |
| P860004/S148
3/22/11 |
SynchroMed II Infusion Pump | Medtronic Neuromodulation
Minneapolis, MN 55432 |
Addition of two new laser welding workstations and two new laser power supplies to the manufacturing process of the Implantable SynchroMed II Infusion Pump, Model 8637. |
| P860057/S076
3/3/11 |
Carpentier-Edwards PERIMOUNT® Pericardial Bioprostheses Heart Valve | Edwards Lifesciences, LLC
Irvine, CA 92614 |
Addition of a new vessel for the Gluteraldehyde mixing process. |
| P870072/S047
3/10/11 |
Thoratec® Ventricular Assist Device (VAD) Surgical Implant Accessory Kit | Thoratec Corporation
Pleasanton, CA 94588 |
Moving a manufacturing process in-house from a contract manufacturer. |
| P880047/S014
3/2/11 |
Gynecare Interceed Absorbable Adhesion Barrier | Ethicon, Inc.
Somerville, NJ 08876 |
Change in the density limit for irradiation shippers. |
| P890003/S215
3/17/11 |
Prodigy IPG | Medtronic, Inc. Mounds View, MN 55112 | Update to the sterile packaging operation process. |
| P890003/S216
3/30/11 |
CapSure, CapSure Model, Service Kit | Medtronic, Inc.
Mounds View, MN 55112 |
Update to the sterile packaging operation process. |
| P890064/S025
3/29/11 |
digene® Hybrid Capture 2 (HC2) HPV DNA Test and digene® Hybrid Capture 2 (HC2) High Risk HPV DNA Test | QIAGEN Gaithersburg, Inc.
Gaithersburg, MD 20878 |
Changes for digene® Hybrid Capture 2 (HC2) HPV DNA Test and digene® Hybrid Capture 2 (HC2) High Risk HPV DNA Test located in Gaithersburg, MD. |
| P900061/S099
3/30/11 |
Accessory – Upsizing Sleeve, Lead End Pin Cap | Medtronic, Inc.
Mounds View, MN 55112 |
Update to the sterile packaging operation process. |
| P910007/S027
3/7/11 |
ARCHITECT Total PSA | Abbott Laboratories
Abbott Park, IL 60064 |
Change in the vendor of antifoam raw material for use in the ARCHITECT Total PSA. |
| P920015/S073
3/30/11 |
Sprint Quattro, Subcutaneous Lead, Transvene SVC Lead | Medtronic, Inc.
Mounds View, MN 55112 |
Update to the sterile packaging operation process. |
| P930014/S047
3/9/11 |
AcrySof ReSTOR Intraocular Lenses and AcrySof IQ Toric Intraocular Lenses | Alcon Research, Ltd.
Fort Worth, TX 76134 |
Implementation of a software modification to enhance and improve intraocular lens production. |
| P930039/S048
3/30/11 |
CapSure, SureFix, Vitatron Crystalline ActFix, Vitatron Pirouet S+ | Medtronic, Inc.
Mounds View, MN 55112 |
Update to the sterile packaging operation process. |
| P940015/S020
3/18/11 |
Synvisc® and Synvisc-One® | Genzyme Corporation
Cambridge, MA 02142 |
Filling of an investigational drug on the INOVA filler machine, which is also used for filling the Synvisc® and Synvisc-One® products. |
| P950005/S032
3/3/11 |
Webster Electrophysiology Catheter, CELSIUS Ablation Catheter | Biosense Webster, Inc.
Diamond Bar, CA 91765 |
Addition of a supplier for catheter tip electrodes. |
| P950008/S008
3/10/11 |
SILIKON 1000 | Alcon Research Ltd.
Fort Worth, TX 76134 |
Establish ISO classification for two controlled environment areas. |
| P950024/S028
3/30/11 |
CapSure Epicardial Pacing | Medtronic, Inc.
Mounds View, MN 55112 |
Update to the sterile packaging operation process. |
| P950029/S057
3/3/11 |
REPLY SR/DR and ESPIRIT SR/DR Implantable Pacemakers | ELA Medical, Inc./ Sorin Group
Plymouth, MN 55441 |
Removal of a hybrid baking step, and the addition of a hybrid cleaning step. |
| P960004/S048
3/24/11 |
THINLINE® II STEROX, FINELINE® II STEROX and FINELINE® II STEROX EZ | Boston Scientific Corporation
St. Paul, MN 55112 |
Change from a scrub method of cleaning a lead body to a wipe method. |
| P960009/S109
3/9/11 |
Activa® Implantable Neurostimulators | Medtronic, Inc.
Minneapolis, MN 55432 |
Implementation of an additional automated plating line at the plating supplier. |
| P960009/S110
3/9/11 |
Soletra®, Kinetra® Activa® PC and Activa® RC | Medtronic, Inc.
Minneapolis, MN 55432 |
Modification to epoxy dispense equipment parameters. |
| P960009/S111
3/17/11 |
Activa SC INS, Soletra INS, Kinetrea INS, Pocket Adaptors | Medtronic Neuromodulation
Minneapolis, MN 55432 |
Addition of a new manufacturing mold and component supplier. |
| P960022/S008
3/28/11 |
SofLens66 and SofLens Toric (alphafilcon A) Soft Contact Lenses | Bausch & Lomb, Inc.
Rochester, NY 14609 |
Change with the supplier of the raw material processing for the SofLens66 and SofLens Toric (alphafilcon A) Soft Contact Lenses. |
| P960042/S028
3/7/11 |
SLS II Spectranetics Laser Sheaths | Spectranetics Corporation
Colorado Springs, CO 80921 |
Change the process for dispensing fluid adhesive from a manual method to a semi-automated method. |
| P970003/S122
3/2/11 |
VNS Therapy® System | Cyberonics, Inc.
Houston, TX 77058 |
Addition of a cleaning step for the Printed Circuit Board. |
| P970003/S123
3/25/11 |
VNS Therapy® System | Cyberonics, Inc.
Houston, TX 77058 |
Change to the pulse generator manufacturing process. |
| P970004/S105
3/9/11 |
InterStim® Implantable Neurostimulators | Medtronic, Inc.
Minneapolis, MN 55432 |
Implementation of an additional automated plating line at the plating supplier. |
| P970004/S106
3/9/11 |
InterStim® and InterStim® II INS | Medtronic, Inc.
Minneapolis, MN 55432 |
Modification to epoxy dispense equipment parameters. |
| P970004/S107
3/17/11 |
InterStim INS | Medtronic Neuromodulation
Minneapolis, MN 55432 |
Addition of a new manufacturing mold and component supplier. |
| P970008/S055
3/2/11 |
Urologix Targis System for the Treatment of BPH | Urologix, Inc.
Minneapolis, MN 55447 |
Removal of a tube trimming step and move the Control Unit keyboard assembly process in house. |
| P970012/S083
3/18/11 |
Kappa 400 | Medtronic, Inc.
Mounds View, MN 55112 |
New mold and an additional supplier for seal components. |
| P970013/S039
3/30/11 |
Microny Family of Pacemakers | St. Jude Medical – CRMD
Sylmar, CA 91342 |
Alternate supplier for pace wires. |
| P970020/S061
3/18/11 |
Multi-Link Zeta RX Coronary Stent System | Abbott Vascular
Temecula, CA 92591 |
Change in resin verification at receiving inspection. |
| P970037/S004
3/4/11 |
AutoDELFIA®/ DELFIA Xpress hAFP | PerkinElmer, Inc. Indianapolis, IN
46236 |
Change in the supplier of a raw material. |
| P970051/S067
3/2/11 |
Nucleus 24 Cochlear Implant System | Cochlear Americas Centennial, CO 80111 | Changes to the manufacturing process for the use of new silicone injection molding equipment. |
| P980007/S018
3/7/11 |
ARCHITECT Free PSA | Abbott Laboratories
Abbott Park, IL 60064 |
Change in the vendor of antifoam raw material for use in the ARCHITECT Free PSA assays. |
| P980016/S278
3/2/11 |
Secura DR/VR, Maximo II DR/VR, and Virtuoso II DR/VR ICDs | Medtronic, Inc. Mounds View, MN 55112 | Change in supplier component testing. |
| P980016/S281
3/17/11 |
Secura DR/VR, Maximo II DR/VR, Virtuoso II DR/VR/V ICDs | Medtronic, Inc.
Mounds View, MN 55112 |
Implementation of a new device manufacturing assembly line. |
| P980016/S282
3/24/11 |
Secura DR/VR, Maximo II DR/VR, Virtuoso II DR/VR ICDs | Medtronic, Inc. Mounds View, MN 55112 | Addition of a dry plasma oxygen clean process step. |
| P980016/S283
3/18/11 |
Marquis, Maximo | Medtronic, Inc.
Mounds View, MN 55112 |
New mold and an additional supplier for seal components. |
| P980016/S284
3/17/11 |
Secura DR/VR ICD, Virtuoso II DR/VR, Maximo II DR/VR, Entrust ICD, Virtuoso ICD | Medtronic, Inc.
Mounds View, MN 55112 |
Update to the sterile packaging operation process. |
| P980016/S285
3/31/11 |
Maximo II, Secura, Virtuoso II ICDs | Medtronic, Inc.
Mounds View, MN 55112 |
Addition of a new equipment controller for the print label files. |
| P980022/S095
3/30/11 |
Continuous Glucose Monitoring System, SOF-Sensor, Glucose Sensors | Medtronic MiniMed Northridge, CA
91325 |
Change to use a semi-automated tape application during sensor base assembly. |
| P980035/S203
3/3/11 |
Adapta, Relia, Sensia, Versa IPGs | Medtronic, Inc.
Mounds View, MN 55112 |
Implementation of a new release of traceability software. |
| P980035/S204
3/24/11 |
Adapta, Versa, Sensia, Relia IPGs | Medtronic, Inc. Mounds View, MN 55112 | Addition of a dry plasma oxygen clean process step. |
| P980035/S205
3/18/11 |
350 Series, Adapta, EnPulse, Kappa 600/650/700/800/ 900, Sigma | Medtronic, Inc.
Mounds View, MN 55112 |
New mold and an additional supplier for seal components. |
| P980035/S206
3/17/11 |
Adapta/Versa/ Sensia IPG Family, Relia IPG and EnRhythm IPG | Medtronic, Inc. Mounds View, MN 55112 | Update to the sterile packaging operation process. |
| P980035/S207
3/31/11 |
Adapta, Relia, Sensia, Versa IPGs | Medtronic, Inc.
Mounds View, MN 55112 |
Addition of a new equipment controller for the print label files. |
| P980049/S063
3/31/11 |
Isoline 2CT and Isoline 2CR Leads | ELA Medical, Inc. Plymouth, MN
55441 |
Update to the current leads label printing software. |
| P980050/S058
3/30/11 |
Transvene CS/SVC | Medtronic, Inc.
Mounds View, MN 55112 |
Update to the sterile packaging operation process. |
| P990001/S085
3/31/11 |
Vitatron DA+C, Vitatron DA+T Series IPGs | Medtronic, Inc.
Mounds View, MN 55112 |
Addition of a new equipment controller for the print label files. |
| P990004/S021
3/2/11 |
Surgifoam Absorbable Gelatin Sponge, U.S.P. | Ethicon, Inc.
Somerville, NJ 08876 |
Change in packaging line equipment. |
| P990009/S031
3/16/11 |
Floseal Hemostatic Matrix | Baxter Healthcare Corporation
McGaw Park, IL 60085 |
Changes in the manufacturing methods or processes. |
| P990025/S027
3/3/11 |
NAVISTAR RMT Catheter | Biosense Webster, Inc.
Diamond Bar, CA 91765 |
Addition of a supplier for catheter tip electrodes. |
| P000010/S020
3/22/11 |
AMPLICOR HCV Test, v.2.0/COBAS AMPLICOR HCV Test v2.0 | Roche Molecular Systems, Inc.
Pleasanton, CA 94588 |
Discontinuation of Final Bulk Testing requirements for bulk Quantitation Standard (QS) and Internal Control (IC) reagents for 17 QS/IC products used with the associated assays. |
| P000012/S029
3/22/11 |
COBAS AmpliPrep /COBAS AMPLICOR HCV Test v2.0 | Roche Molecular Systems, Inc.
Pleasanton, CA 94588 |
Discontinuation of Final Bulk Testing requirements for bulk Quantitation Standard (QS) and Internal Control (IC) reagents for 17 QS/IC products used with the associated assays. |
| P000014/S023
3/10/11 |
VITROS Immunodiagnostic Products Anti-HBs Reagent Pack and Calibrator | Ortho-Clinical Diagnostics
Rochester, NY 14626 |
Change to manufacture and store the antifoam solution used in VITROS Anti-HBs Conjugate Reagent. |
| P000020/S014
3/17/11 |
Stinger, Stinger S, Stinger M, Stinger SM, Scorpion 2 and Scorpion 2M Ablation Catheters and Templink/ Templink M Extension Cables | C.R. Bard, Inc.
Lowell, MA 01851 |
Addition of a new supplier for connector assemblies and plug cable connectors. |
| P010014/S030
3/24/11 |
Oxford Partial Knee System | Biomet, Inc.
Warsaw, IN 46581 |
Change to the heat sealing of blister packs procedure by adding a new benchtop sealer. |
| P010015/S109
3/30/11 |
Attain | Medtronic, Inc.
Mounds View, MN 55112 |
Update to the sterile packaging operation process. |
| P010019/S020
3/16/11 |
CIBA VISION (lotrafilcon B) Soft Contact Lenses | CIBA VISION Corporation
Duluth, GA 30097 |
Change the endotoxin testing site to the CIBA VISION Johor Microbiology Laboratory in Johor, Malaysia. |
| P010023/S008
3/2/11 |
Maxum System | Ototronix, LLC
St. Paul, MN 55110 |
Change to the IPC shell fabrication process. |
| P010030/S026
3/28/11 |
LifeVest Wearable Cardioverter | ZOLL Lifecor Corporation
Pittsburgh, PA 15238 |
Addition of a new thermoforming machine. |
| P010031/S234
3/2/11 |
Concerto CRT-D, Maximo II CRT-D, and Concerto II ICD | Medtronic, Inc.
Mounds View, MN 55112 |
Change in supplier component testing. |
| P010031/S236
3/17/11 |
Concerto, Concerto II ICD, Consulta CRT-D, Maximo II CRT-D | Medtronic, Inc.
Mounds View, MN 55112 |
Implementation of a new device manufacturing assembly line. |
| P010031/S237
3/24/11 |
Concerto II ICD, Consulta, Maximo II CRT-Ds | Medtronic, Inc. Mounds View, MN 55112 | Addition of a dry plasma oxygen clean process step. |
| P010031/S238
3/17/11 |
InSync Sentry CRT-D, Concerto ICD, Consulta CRT-D, Concerto II CRT-D, Maximo II CRT-D | Medtronic, Inc. Mounds View, MN 55112 | Update to the sterile packaging operation process. |
| P010031/S239
3/31/11 |
Concerto II, Consulta, Maximo II CRT-Ds | Medtronic, Inc.
Mounds View, MN 55112 |
Addition of a new equipment controller for the print label files. |
| P010068/S022
3/3/11 |
CELSIUS DS Ablation Catheter | Biosense Webster, Inc.
Diamond Bar, CA 91765 |
Addition of a supplier for catheter tip electrodes. |
| P020004/S059
3/16/11 |
GORE EXCLUDER® AAA Endoprosthesis | W.L. Gore & Associates, Inc.
Flagstaff, AZ 86003 |
Removal of a cooling chamber and an update to the touch screen software. |
| P020004/S060
3/18/11 |
GORE EXCLUDER® AAA Endoprosthesis | W.L. Gore & Associates, Inc.
Flagstaff, AZ 86003 |
Automation of a trimming process. |
| P020030/S008
3/31/11 |
Stelix BR, Stelix II BRF, and Stelid II BTF/BJF Leads | ELA Medical, Inc. Plymouth, MN
55441 |
Update to the current leads label printing software. |
| P020047/S030
3/18/11 |
Multi-Link Vision and Multi-Link Mini Vision OTW and RX Coronary Stent System | Abbott Vascular
Temecula, CA 92591 |
Change in resin verification at receiving inspection. |
| P020047/S031
3/18/11 |
Multi-Link Vision®, Multi-Link Mini Vision®, Multi-Link 8™, Multi-Link 8™ LL and Multi-Link 8™ SV Coronary Stent Systems | Abbott Vascular Temecula, CA 92591 | Change in quality control testing for balloon rupture. |
| P030002/S023
3/29/11 |
Crystalens® Accomodating Intraocular Lens | Bausch & Lomb, Inc.
Aliso Viejo, CA 92656 |
Relocation of the final inspection and pre-pack operation at the manufacturing facility located in Rancho Cucamonga, California. |
| P030017/S116
3/28/11 |
Precision® Spinal Cord Stimulator System | Boston Scientific Corporation
Valencia, CA 91355 |
Addition of an alternate assembly method for the leads and extensions for the Precision® Spinal Cord Stimulator (SCS) System. |
| P030017/S117
3/30/11 |
Precision® Spinal Cord Stimulator (SCS) System | Boston Scientific Corporation
Valencia, CA 91355 |
Addition of pouch sealing equipment for the in-house processing of products packaged in Tyvek pouches. |
| P030029/S012
3/14/11 |
ADVIA Centaur Anti-HBs Assay | Siemens Healthcare Diagnostics
East Walpole, MA 02032 |
Change of raw material used in the production of the Lite Reagent buffer. |
| P030036/S026
3/30/11 |
SelectSecure | Medtronic, Inc.
Mounds View, MN 55112 |
Update to the sterile packaging operation process. |
| P040012/S037
3/30/11 |
Acculink Carotid Stent System | Abbott Vascular, Inc.
Santa Clara, CA 95054 |
Changes to the in- process inspection and specification for the Inner Member (IM) to hypotube bond of the device. |
| P040012/S038
3/30/11 |
Acculink Carotid Stent System | Abbott Vascular, Inc.
Santa Clara, CA 95054 |
Addition of an alternate heat sealer. |
| P040016/S070
3/18/11 |
VeriFLEX (Liberté) Coronary Stent System | Boston Scientific Corporation
Maple Grove, MN 55311 |
Change in bacterial endotoxin test methodology. |
| P040020/S030
3/9/11 |
AcrySof ReSTOR and AcrySof IQ Toric Intraocular Lenses | Alcon Research, Ltd.
Fort Worth, TX 76134 |
Implementation of a software modification to enhance and improve intraocular lens production. |
| P040038/S021
3/30/11 |
Xact® Carotid Stent System | Abbott Vascular, Inc.
Santa Clara, CA 95054 |
Addition of an alternate heat sealer. |
| P040043/S038
3/16/11 |
GORE® TAG® Thoracic Endoprosthesis | W.L. Gore & Associates, Inc.
Flagstaff, AZ 86003 |
Removal of a cooling chamber and an update to the touch screen software. |
| P040044/S036
3/10/11 |
Mynx® Vascular Closure Device | Access Closure, Inc. Mountain View, CA
94043 |
Addition of a supplier for subassemblies of the Mynx product family. |
| P050012/S036
3/2/11 |
DexCom Seven and Seven Plus Continuous Glucose Monitoring System | DexCom Inc.
San Diego, CA 92121 |
Alternate Vendor and method of manufacture of the disposable seal component of the applicator assembly of the Seven and Seven Plus systems. The proposed change applies only to the disposable seal supplier and the method of manufacture; neither the materials nor the final design of the disposable seal are altered. Sensor performance and release specification will also remain unchanged. |
| P050020/S033
3/10/11 |
Freestyle Navigator Continuous Glucose Monitoring System | Abbott Diabetes Care, Inc.
Alameda, CA 04502 |
Addition of an alternate supplier of the injection molded components of the Freestyle Navigator Continuous Glucose Monitoring System. |
| P050028/S016
3/22/11 |
COBAS TaqMan HBV Test for use with The High Pure System | Roche Molecular Systems, Inc.
Pleasanton, CA 94588 |
Discontinuation of Final Bulk Testing requirements for bulk Quantitation Standard (QS) and Internal Control (IC) reagents for 17 QS/IC products used with the associated assays. |
| P050034/S005
3/31/11 |
Implantable Miniature Telescope (IMT) | VisionCare Ophthalmic Technologies, Inc. Saratoga, CA
95070 |
Change to the biological indicator used in the sterilization process and to add an option for a second full cycle sterilization (double sterilization) to the manufacturing process if required. |
| P050051/S010
3/23/11 |
ARCHITECT AUSAB | Abbott Laboratories Abbott Park, IL
60064 |
Changes in two quality control test methods used for in-process testing of bulk components. |
| P060007/S008
3/30/11 |
ARCHITECT HBsAg and ARCHITECT HBsAg Confirmatory Assays | Abbott Laboratories Abbott Park, IL 60064 | Specification change for the negative human plasma for the HBsAg assays. |
| P060007/S009
3/30/11 |
ARCHITECT HBsAg and ARCHITECT HBsAg Confirmatory Assays | Abbott Laboratories Abbott Park, IL 60064 | Test method conversions for calf bovine serum for the two HBsAg assays. |
| P060007/S010
3/30/11 |
ARCHITECT HBsAg and ARCHITECT HBsAg Confirmatory Assays | Abbott Laboratories Abbott Park, IL 60064 | Plasma test method conversions for ARCHITECT HBsAg and ARCHITECT HBsAg Confirmatory Assays. |
| P060007/S011
3/30/11 |
ARCHITECT HBsAg and ARCHITECT HBsAg Confirmatory Assays | Abbott Laboratories Abbott Park, IL 60064 | Test method change for quantitating Anti-D and Anti-Y monoclonal antibodies which are used in the testing of the recombinant HBsAg subtype Ad (Code 98034) and HBsAg subtype Ay (Code 98035) antigens used in the ARCHITECT HBsAg and HBsAg Confirmatory assays. |
| P060011/S001
3/31/11 |
C-flex Intraocular Lens | Rayner Intraocular Lenses Limited
East Sussex, England, U.K. BN37AN |
Alternative optical measurement equipment. |
| P060027/S030
3/31/11 |
Situs OTW UW28D Lead | ELA Medical, Inc. Plymouth, MN
55441 |
Update to the current leads label printing software. |
| P060030/S017
3/22/11 |
COBAS AmpliPrep/ COBAS TaqMan HCV Test and COBAS TaqMan HCV Test for use with The High Pure System, v2.0 | Roche Molecular Systems, Inc.
Pleasanton, CA 94588 |
Discontinuation of Final Bulk Testing requirements for bulk Quantitation Standard (QS) and Internal Control (IC) reagents for 17 QS/IC products used with the associated assays. |
| P060039/S022
3/30/11 |
Attain StarFix | Medtronic, Inc.
Mounds View, MN 55112 |
Update to the sterile packaging operation process. |
| P070007/S028
3/3/11 |
Talent Thoracic Stent Graft System | Medtronic Vascular Santa Rosa, CA
95403 |
Addition of a lubricant during assembly of the Captiva Delivery System. |
| P070007/S030
3/18/11 |
Talent Thoracic Stent Graft System with Captiva Delivery System | Medtronic Ireland
Galway, Ireland |
Transfer of post sterilization inspections to an alternate site. |
| P070015/S056
3/3/11 |
XIENCE V® Everolimus Eluting Coronary Stent System | Abbott Vascular Temecula, CA
92591 |
Change to the coating manufacturing process. |
| P070015/S059
3/18/11 |
XIENCE V® and PROMUS Everolimus Eluting Coronary Stent System | Abbott Vascular
Temecula, CA 92591 |
Change in resin verification at receiving inspection. |
| P070022/S012
3/9/12 |
Adiana Permanent Contraception System | Hologic, Inc.
Marlborough, MA 01752 |
Addition of a manufacturing step for the Adiana matrix component. |
| P080006/S020
3/30/11 |
Attain Ability | Medtronic, Inc.
Mounds View, MN 55112 |
Update to the sterile packaging operation process. |
| P090003/S009
3/9/11 |
Express™ LD Iliac Premounted Stent System | Boston Scientific Maple Grove, MN
55311 |
Modification in the balloon wingfolding operation during manufacture of the device. |
| P090003/S010
3/18/11 |
Express LD Iliac Premounted Stent Systems | Boston Scientific Corporation
Maple Grove, MN 55311 |
Change in bacterial endotoxin test methodology. |
| P090006/S005
3/18/11 |
Complete SE Vascular Stent System | Medtronic Ireland
Galway, Ireland |
Transfer of post sterilization inspections to an alternate site. |
| P090013/S001
3/18/11 |
REVO MRI™ SureScan® Pacing System | Medtronic, Inc.
Mounds View, MN 55112 |
Multiple changes in suppliers of various electronic components. |
| P090013/S002
3/17/11 |
REVO MRI™ SureScan® Pacing System | Medtronic, Inc. Mounds View, MN 55112 | Update to the sterile packaging operation process. |
| P090013/S003
3/25/11 |
REVO MRI™ SureScan® Pacing System | Medtronic, Inc.
Mounds View, MN 55112 |
Upgrades to various manufacturing process software versions. |
| P090013/S004
3/30/11 |
CapSure Fix | Medtronic, Inc.
Mounds View, MN 55112 |
Update to the sterile packaging operation process. |
| P090013/S005
3/28/11 |
REVO MRI™ SureScan® Pacing System | Medtronic, Inc.
Mounds View, MN 55112 |
Changes to align production with existing processes used in other marketed devices. |
| P090013/S007
3/31/11 |
Revo MRI™ SureScan® Pacing System | Medtronic, Inc.
Mounds View, MN 55112 |
Revising parameters to an epoxy dispense manufacturing process. |
| P090013/S008
3/31/11 |
Revo MRI IPG | Medtronic, Inc.
Mounds View, MN 55112 |
Addition of a new equipment controller for the print label files. |
| P100010/S003
3/9/11 |
Arctic Front Cardiac CryoAblation Catheter | Medtronic Cryocath LP
Quebec, Canada H9R 5ZB |
Change of the adhesive used to seal the vacuum tube to rear strain. |
| P100021/S005
3/16/11 |
Endurant® Stent Graft System | Medtronic Vascular
Santa Rosa, CA 95403 |
Addition of an automated crimping machine used during the radiopaque marker- band bond process of the Endurant Delivery System. |
| P100021/S006
3/18/11 |
Endurant® Stent Graft System | Medtronic Ireland Galway, Ireland | Transfer of post sterilization inspections to an alternate site. |
| P100021/S007
3/18/11 |
Endurant® Stent Graft System | Medtronic Ireland Galway, Ireland | Improvements upon the current process for stent graft loading. |
Summary of PMA Originals & Supplements Approved
Originals: 2
Supplements: 89
Summary of PMA Originals Under Review
Total Under Review: 96
Total Active: 47
Total On Hold: 49
Number Greater Than 180 Days: 4
Summary of PMA Supplements Under Review
Total Under Review: 654
Total Active: 457
Total On Hold: 197
Number Greater Than 180 Days: 11
Summary of All PMA Submissions Received
Originals: 3
Supplements: 97
Summary of PMA Supplement PMA Approval/Denial Decision Times
Number of Approvals: 89
Number of Denials: 0
Average Days Fr Receipt to Decision (Total Time): 210.8
FDA Time: 122.4 Days MFR Time: 88.4 Days
