CYPHER SELECT® Plus Sirolimus-eluting Coronary Stent Now Approved In The EU For Treatment Of Patients With Diabetes

The CYPHER SELECT®Plus Sirolimus-eluting Coronary Stent has received CE marking within the European Union for treatment of patients with diabetes, a complex and often difficult-to-treat patient population.

Edwards Lifesciences Receives CE Mark For New Transfemoral Transcatheter Valve Delivery System

Edwards Lifesciences Corporation announced today that it received CE Mark approval for European commercial sales of the new RetroFlex 3 transfemoral delivery system for the Edwards SAPIEN transcatheter heart valve.

St. Jude Medical Announces U.S. Approval of Industry’s First Connector System Designed to Simplify Implant Process for Cardiac Resynchronization Therapy Devices

New lead and cardiac resynchronization system design is expected to offer implanting physicians a simpler and quicker procedure and reduces the volume of the leads and device in the chest pocket for heart failure patients

Small Bone Innovations, Inc. Completes Acquisition Of S.T.A.R. Total Ankle Replacement System

Small Bone Innovations, Inc. (SBi) announced today that it has completed the acquisition of Link America, Inc., d/b/a Link Orthopaedics, The Scandinavian Total Ankle Replacement system, known as the ‘S.T.A.R.® Ankle’, and certain assets related to the S.T.A.R. Ankle.

St. Jude Medical Announces European CE Mark Approval For Libra Deep Brain Stimulation Systems For Parkinson’s Disease

St. Jude Medical, Inc. announced European CE Mark approval of its Libra® and LibraXP™ deep brain stimulation systems for treating the symptoms of Parkinson’s disease, a neurological disorder that progressively diminishes a person’s control over his or her movements and speech.

Most read

Latest

^