FDA Approves First Percutaneous Heart Valve

The U.S. Food and Drug Administration approved the Medtronic Melody Transcatheter Pulmonary Valve and Ensemble Delivery System, the first heart valve to be implanted through a catheter, or tube, in a leg vein and guided up to the heart. This new approach to the treatment of adults and children with previously implanted, poorly functioning pulmonary [...]

Melody(R) Transcatheter Valve Demonstrates Encouraging Results In Study On Patients With Congenital Heart Disease

Clinical trial results published in this week’s Journal of the American College of Cardiology (JACC) describe six-month outcomes for patients using the Melody® Transcatheter Pulmonary Valve from Medtronic, Inc. (NYSE: MDT). The valve is implanted through a catheter procedure instead of open-heart surgery in patients with congenital heart disease affecting the function of their pulmonary [...]

Leading Cardiovascular Surgeons Gather From Around The World To Share Ross Procedure Survival Data, Techniques At 2nd Annual Summit

Elite cardiovascular surgeons from around the world will travel to suburban Atlanta this week for the two-day Ross Summit to review and discuss current peer-reviewed data relating to the survival advantage of the Ross Procedure and to practice the technical nuances required to perform this heart surgery successfully.

CryoLife’s Second Annual Surgical Congress For The Ross Procedure To Draw More Than 130 Cardiovascular Surgeons From Around The World

More than 130 cardiovascular surgeons from approximately 30 countries are scheduled to attend the second annual global Ross Summit, a two-day surgical congress focused on the highly complex Ross Procedure, which is performed on up to 1,500 individuals globally each year — a number that is expected to increase as survival data become more widely [...]

FDA Clears New Immune Response Claim For The CryoValve(R) SG Pulmonary Human Heart Valve

CryoLife, Inc. (NYSE: CRY), a biomaterials, medical device and tissue processing company, announced that the U.S. Food and Drug Administration (FDA) has cleared a new claim for the CryoValve(R) SG pulmonary human heart valve. The new labeling claim relates to reducing a component of the immune response in recipients of the CryoValve SG.