Press Release
Press Release: FDA approves the Syncardia total artificial heart with Synhall valves
Press Release: Transluminal Technologies receives CE Mark approval for velox CD vascular closure device
Press Release: Vittamed received CE Mark approval for non-invasive intracranial pressure meter and non-invasive cerebrovascular autoregulation monitor
Press Release: Medtronic receives FDA approval for prestige LP cervical disc system
MEMPHIS, TENN. – Medtronic, Inc. (NYSE: MDT) announces that it has received approval from the U.S. Food and Drug Administration (FDA) to market the PRESTIGE® LP Cervical Disc System for the treatment of single-level cervical disc disease (radiculopathy and/or myelopathy).
Press Release: Guided Therapeutics files PMA Amendment with FDA for LuViva Advanced Cervical Scan
NORCROSS, Ga. — Guided Therapeutics, Inc. (OTCBB: GTHP) (OTCQB: GTHP) today announced that it has filed an amendment to its premarket approval (PMA) application with the U.S. Food and Drug Administration (FDA) for the LuViva Advanced Cervical Scan.
Press Release: Sorin Group announces CE Mark approval for Crown PRT heart valve
Milan, Italy – Sorin Group, (Reuters Code: SORN.MI), a global medical device company and a leader in the treatment of cardiovascular diseases, announced today it has been granted CE mark certification for its innovative stented aortic bioprosthesis Crown PRT, now commercially available in Europe.