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Revascularization with OrbusNeich’s Genous™ Stent May Enable the Safe and Early Discontinuation of Dual Antiplatelet Therapy for Patients with Increased Bleeding Risk

October 12, 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

Eurocor’s DEBIFU Registry successfully enrolled first patients

September 24, 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

Boston Scientific Announces Expanded Indication For CRE Wireguided Balloon Dilator

May 29, 2012

News Industry News

Boston Scientific Announces FDA Approval and U.S. Launch of EPIC™ Vascular Stent

May 17, 2012

News Industry News

Boston Scientific Announces Positive Data From Lotus™ Transcatheter Aortic Valve Trial

May 15, 2012

News Industry News

Boston Scientific Announces CE Mark and European Launch of Innova™ Self-expanding Bare-metal Stent System

May 14, 2012

News Industry News

Boston Scientific Completes Enrollment in Clinical Trial to Evaluate Lotus™ Aortic Valve System

April 23, 2012

News Industry News

OrbusNeich’s Genous™ Stent Achieves Complete Endothelialization at Two Weeks

April 20, 2012

News Industry News

St. Jude Medical Launches New Trifecta Heart Valve in Japan

April 17, 2012

News Industry News

FDA Panel Scheduled to Review Edwards SAPIEN Valve for High-Risk Patients on June 13

April 09, 2012

News Industry News

Edwards Lifesciences Files Official Comment on CMS' Proposed TAVR National Coverage Determination

March 04, 2012

News Industry News

Medtronic Completes Enrollment of Extreme Risk Patient Group in CoreValve® U.S. Pivotal Trial

January 23, 2012

News Industry News

First Patient Enrolled in Medtronic-Supported Head-To-Head Clinical Trial Comparing Cryoballoon Ablation to RF Ablation for Paroxysmal Atrial Fibrillation

January 23, 2012

News Industry News

Bard Acquires Lutonix, Inc.

December 19, 2011

News Industry News

St. Jude Medical Announces First Implant in European Clinical Trial Studying Portico Transcatheter Aortic Heart Valve

December 12, 2011

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Revascularization with OrbusNeich’s Genous™ Stent May Enable the Safe and Early Discontinuation of Dual Antiplatelet Therapy for Patients with Increased Bleeding Risk

First Patient Enrolled in REPRISE II TAVR Clinical Trial to Evaluate the Safety and Performance of the Lotus™ Valve System

New Data Reinforce Positive Clinical Outcomes for Direct Aortic Implants Using the Medtronic CoreValve System

Eurocor’s DEBIFU Registry successfully enrolled first patients

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

Medtronic Begins Global Clinical Trial Evaluating CoreValve® System Implantation in Intermediate-Risk Patients

FDA Panel Recommends Approval of Edwards Transcatheter Valve for High-Risk Patients

Boston Scientific Announces Expanded Indication For CRE Wireguided Balloon Dilator

Boston Scientific Announces FDA Approval and U.S. Launch of EPIC™ Vascular Stent

Boston Scientific Announces Positive Data From Lotus™ Transcatheter Aortic Valve Trial

Boston Scientific Announces CE Mark and European Launch of Innova™ Self-expanding Bare-metal Stent System

Boston Scientific Completes Enrollment in Clinical Trial to Evaluate Lotus™ Aortic Valve System

OrbusNeich’s Genous™ Stent Achieves Complete Endothelialization at Two Weeks

St. Jude Medical Launches New Trifecta Heart Valve in Japan

FDA Panel Scheduled to Review Edwards SAPIEN Valve for High-Risk Patients on June 13

Edwards Lifesciences Files Official Comment on CMS' Proposed TAVR National Coverage Determination

Medtronic Completes Enrollment of Extreme Risk Patient Group in CoreValve® U.S. Pivotal Trial

First Patient Enrolled in Medtronic-Supported Head-To-Head Clinical Trial Comparing Cryoballoon Ablation to RF Ablation for Paroxysmal Atrial Fibrillation

Bard Acquires Lutonix, Inc.

St. Jude Medical Announces First Implant in European Clinical Trial Studying Portico Transcatheter Aortic Heart Valve

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