
Boston Scientific Corp.’s (NYSE:BSX) Alair asthma management system won reimbursement from the Centers for Medicare & Medicaid Services, effective at the start of this year.
The Alair system delivers precise thermal energy lung to tissue via bronchoscope to reduce excessively smooth muscle, decreasing the airway’s ability to constrict.
The federal agency granted the Alair device approval for Medicare reimbursement through a separate "pass-through" payment when the procedure is performed in outpatient settings, the Natick, Mass.-based med-tech titan announced.
Sign up to get our free newsletters delivered right to your inbox
The approval allows hospitals to receive payment for the Alair catheter in addition to Medicare payment for the bronchial thermoplasty procedure, according to a press release.
"CMS’ decision that the Alair bronchial thermoplasty system meets the criteria for transitional pass-through payment is a very positive development for severe asthmatics and the pulmonary physician community," BSX endoscopy division president David Pierce said in prepared remarks."It supports what we have confirmed through our clinical trials: bronchial thermoplasty offers a new advancement in the treatment of patients with severe asthma who are not well controlled despite taking recommended doses of asthma medications. This decision also sets an important precedent for health care payers throughout the United States."
Boston Scientific added the Alair system to its portfolio when it acquired Asthmatx Inc. for $194 million in Sept. 2010. Alair won FDA approval in April 2010, becoming the first device-based asthma treatment approved by the watchdog agency.

BioMimetic’s bone graft PMA gets a no-go from the FDA
The federal watchdog agency did not approve the pre-market approval application for BioMimetic Therapeutics’ Augment bone graft, even after an independent advisory panel voted in the product’s favor. Read more
AirStrip lands CE Mark for mobile monitoring system
San Antonio, Texas-based AirStrip Technologies won CE Mark approval for its flagship mobile patient monitoring systems. The AirStrip OB, AirStrip Cardiology and AirStrip Patient Monitoring systems are all available for use by European clinicians. Read more
Ultrasound stroke treatment wins CE Mark
Cerevast Therapeutics landed CE Mark approval for its Clotbust ER SonoLysis system to treat ischemic stroke in emergency settings. Read more
FDA approves Cyberonics AspireHC generator
The federal watchdog agency cleared the re-design of Cyberonics Inc.’s AspireHC generator. The VNS therapy treatment was the subject of a voluntary recall in August 2011. Read more
Enteromedics completes enrollment of clinical trials
St. Paul, Minn.-based Enteromedics completed patient enrollment of the ReCharge trial for its VBloc vagal blocking therapy. The random, double-blind, parallel-group study will consist of 233 patients in the U.S. and Australia. Read more
ThermoGenesis wins approval in India
ThermoGenesis Corp. landed approval from India’s Ministry of Health for its AutoXpress system for the processing of stem cells from cord blood. Read more
BioLineRx initiates registration trial for BCM
Biopharmaceutical development company BioLineRx initiated the CE mark registration trial of its BCM (BL-1040) system, a medical device to prevent cardiac remodeling following acute myocardial infarctions. Read more