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Boston Scientific Announces Launch of PROMUS Element™ Platinum Chromium Stent System in Japan

February 29, 2012

News Industry News

EDWARDS INTUITY Valve System Receives CE Mark

February 15, 2012

News Industry News

FDA Advisory Panel Recommends Expanded Indication for Medtronic Cardiac Resynchronization Therapy with Defibrillator (CRT-D) Devices

December 07, 2011

News Industry News

Edwards Receives FDA Approval to Expand U.S. Clinical Trial of Next-Generation Transcatheter Valve

November 06, 2011

News Industry News

Medtronic’s Unmatched Portfolio of Cardiovascular Devices Features Prominently on Program for TCT 2011

November 04, 2011

News Industry News

Edwards Lifesciences Receives FDA Approval for First Catheter-Based Aortic Heart Valve in the U.S.

November 03, 2011

News Industry News

Abbott Receives U.S. FDA Approval for Next-Generation XIENCE PRIME™ Drug Eluting Stent

November 01, 2011

News Daily News

CRF, ACC Partnership Enhances Interventional Education, Science Worldwide

October 31, 2011

News Daily News

First DES for Above-the-Knee Vascular Disease on the Horizon

L.A. McKeown

October 18, 2011

News Industry News

Boston Scientific Launches Promus Element™ Stent System In China

October 17, 2011

News Industry News

Physio-Control Introduces New Basic Life Support 12-Lead ECG Solution

August 24, 2011

News Industry News

Cordis Announces Discontinuation of NEVO Sirolimus-Eluting Coronary Stent

June 15, 2011

News Industry News

Abbott Receives U.S. FDA Approval for XIENCE nano™ to Treat Coronary Artery Disease in Small Vessels

May 24, 2011

News Industry News

St. Jude Medical Announces FDA Approval of Trifecta Valve

April 20, 2011

News Industry News

Boston Scientific Begins International Clinical Trial Enrollment for INNOVA™ Self-Expanding Bare-Metal Stent System

April 05, 2011

News Industry News

Edwards Lifesciences Expands Treatable Patient Population With European Approval of Larger Transcatheter Valve

February 23, 2011

News Industry News

Abbott Receives CE Mark Approval for World's First Drug Eluting Bioresorbable Vascular Scaffold for Treatment of Coronary Artery Disease

January 09, 2011

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July 17, 2020

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Boston Scientific Announces Launch of PROMUS Element™ Platinum Chromium Stent System in Japan

EDWARDS INTUITY Valve System Receives CE Mark

FDA Advisory Panel Recommends Expanded Indication for Medtronic Cardiac Resynchronization Therapy with Defibrillator (CRT-D) Devices

Edwards Receives FDA Approval to Expand U.S. Clinical Trial of Next-Generation Transcatheter Valve

Medtronic’s Unmatched Portfolio of Cardiovascular Devices Features Prominently on Program for TCT 2011

Edwards Lifesciences Receives FDA Approval for First Catheter-Based Aortic Heart Valve in the U.S.

Abbott Receives U.S. FDA Approval for Next-Generation XIENCE PRIME™ Drug Eluting Stent

CRF, ACC Partnership Enhances Interventional Education, Science Worldwide

First DES for Above-the-Knee Vascular Disease on the Horizon

Boston Scientific Launches Promus Element™ Stent System In China

Physio-Control Introduces New Basic Life Support 12-Lead ECG Solution

Cordis Announces Discontinuation of NEVO Sirolimus-Eluting Coronary Stent

Abbott Receives U.S. FDA Approval for XIENCE nano™ to Treat Coronary Artery Disease in Small Vessels

St. Jude Medical Announces FDA Approval of Trifecta Valve

Boston Scientific Begins International Clinical Trial Enrollment for INNOVA™ Self-Expanding Bare-Metal Stent System

Edwards Lifesciences Expands Treatable Patient Population With European Approval of Larger Transcatheter Valve

Abbott Receives CE Mark Approval for World's First Drug Eluting Bioresorbable Vascular Scaffold for Treatment of Coronary Artery Disease

COVID-19 TCTMD HUB

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