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Cardiosolutions, Inc. Gathers Major Investment from Sorin Group

July 10, 2012

News Industry News

Medtronic Stent Graft Chosen by U.S. FDA for Innovative Program

June 21, 2012

News Industry News

Boston Scientific Receives FDA Approval for 32 MM and 38 MM Lengths for PROMUS Element™ Plus Platinum Chromium Stent System

June 04, 2012

News Daily News

JAMA Letter: Damage to DES After Balloon Expansion Documented in All 4 FDA-Approved Devices

May 25, 2012

News Industry News

Medtronic Nets New Indications for Resolute Integrity Drug-Eluting Stent in Europe

May 15, 2012

News Industry News

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

May 15, 2012

News Industry News

ART receives receives regulatory approval to begin First-In-Man “ARTDIVA” clinical trial with its next-generation bioresorbable stent

May 15, 2012

News Daily News

FDA Label Change Fails to Stem Uncertainty Over PPI Use with Clopidogrel

Caitlin E. Cox

May 09, 2012

News Features

FDA Label Change Fails to Stem Uncertainty Over PPI Use with Clopidogrel

Caitlin E. Cox

May 07, 2012

News Industry News

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

April 23, 2012

News Industry News

St. Jude Medical Launches New Trifecta Heart Valve in Japan

April 17, 2012

News Daily News

Action Plan to Optimize Radiation Safety of Cardiovascular Imaging Developed

March 29, 2012

News Daily News

SCAI Publishes Cath Lab Best Practices

March 22, 2012

News Daily News

PLATO Analysis: PPIs Problematic with Both Ticagrelor, Clopidogrel

Caitlin E. Cox

March 06, 2012

News Daily News

Live Case Procedures Just as Safe as in Daily Practice

Caitlin E. Cox

February 21, 2012

News Industry News

TriReme Medical, Inc. Receives FDA 510(K) Clearance For Chocolate PTA Balloon Catheter

December 31, 2011

News Industry News

Berlin Heart‘s EXCOR® Pediatric Ventricular Assist Device (VAD)

December 15, 2011

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

Boston Scientific Receives FDA Approval for PROMUS Element™ Plus Platinum Chromium Stent System

November 21, 2011

News Industry News

REMEDEE Study Meets Primary Endpoint: OrbusNeich’s Combo™ Dual Therapy Stent Is Non-Inferior to DES

November 13, 2011

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Cardiosolutions, Inc. Gathers Major Investment from Sorin Group

Medtronic Stent Graft Chosen by U.S. FDA for Innovative Program

Boston Scientific Receives FDA Approval for 32 MM and 38 MM Lengths for PROMUS Element™ Plus Platinum Chromium Stent System

JAMA Letter: Damage to DES After Balloon Expansion Documented in All 4 FDA-Approved Devices

Medtronic Nets New Indications for Resolute Integrity Drug-Eluting Stent in Europe

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

ART receives receives regulatory approval to begin First-In-Man “ARTDIVA” clinical trial with its next-generation bioresorbable stent

FDA Label Change Fails to Stem Uncertainty Over PPI Use with Clopidogrel

FDA Label Change Fails to Stem Uncertainty Over PPI Use with Clopidogrel

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

St. Jude Medical Launches New Trifecta Heart Valve in Japan

Action Plan to Optimize Radiation Safety of Cardiovascular Imaging Developed

SCAI Publishes Cath Lab Best Practices

PLATO Analysis: PPIs Problematic with Both Ticagrelor, Clopidogrel

Live Case Procedures Just as Safe as in Daily Practice

TriReme Medical, Inc. Receives FDA 510(K) Clearance For Chocolate PTA Balloon Catheter

Berlin Heart‘s EXCOR® Pediatric Ventricular Assist Device (VAD)

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

Boston Scientific Receives FDA Approval for PROMUS Element™ Plus Platinum Chromium Stent System

REMEDEE Study Meets Primary Endpoint: OrbusNeich’s Combo™ Dual Therapy Stent Is Non-Inferior to DES

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