News Industry News FDA Approves Expanded Indication for Edwards Lifesciences' Transcatheter Valve October 19, 2012
News Industry News FDA Approval of Transapical Approach Offers Patients with Severe Aortic Stenosis a New Surgical Option October 19, 2012
News Industry News Minneapolis Heart Institute Foundation Announces Schedule of Events at TCT Conference October 18, 2012
News Industry News Loma Vista Medical receives FDA clearance for its TRUE Dilatation™ Balloon Valvuloplasty Catheter October 17, 2012
News Industry News First Patient Enrolled in REPRISE II TAVR Clinical Trial to Evaluate the Safety and Performance of the Lotus™ Valve System October 10, 2012
News Industry News New Data Reinforce Positive Clinical Outcomes for Direct Aortic Implants Using the Medtronic CoreValve System October 02, 2012
News Industry News Medtronic Completes High Risk Patient Enrollment in CoreValve® U.S. Pivotal Trial and Gains FDA Approval to Study Intermediate Risk Patients in Global SURTAVI Trial September 05, 2012
News Industry News Medtronic Begins Global Clinical Trial Evaluating CoreValve® System Implantation in Intermediate-Risk Patients July 18, 2012
News Industry News FDA Panel Recommends Approval of Edwards Transcatheter Valve for High-Risk Patients June 13, 2012
News Industry News Edwards Receives IDE for U.S. Clinical Trial of New Heart Valve Tissue Treatment Platform June 08, 2012
News Industry News Edwards SAPIEN XT Transcatheter Valve Continues to Achieve Positive Patient Outcomes in 94 Center Post-Approval Study May 17, 2012
News Industry News Key Clinical Data for St. Jude Medical’s Structural Heart Technologies Revealed at EuroPCR May 16, 2012
News Industry News Boston Scientific Announces Positive Data From Lotus™ Transcatheter Aortic Valve Trial May 15, 2012
News Industry News Loma Vista Medical receives CE mark for its TRUE Dilatation™ Balloon Valvuloplasty Catheter May 10, 2012
News Industry News Boston Scientific Completes Enrollment in Clinical Trial to Evaluate Lotus™ Aortic Valve System April 23, 2012
News Industry News FDA Panel Scheduled to Review Edwards SAPIEN Valve for High-Risk Patients on June 13 April 09, 2012