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Boston Scientific Concludes Enrollment In Randomized, Multicenter, Pivotal Study Of SYNERGY™ Coronary Stent System

September 12, 2013

News Industry News

Thoratec Acquires DuraHeart® II Ventricular Assist System

July 01, 2013

News Industry News

Edwards Lifesciences Comments on FDA Warning Letter

May 29, 2013

News Industry News

Boston Scientific Reports Lotus™ Valve System Met Primary Performance Endpoint in REPRISE II Trial

May 22, 2013

News Industry News

First Patient Enrolled in the Boston Scientific Multicenter Study of the SYNERGY™ Coronary Stent System Featuring a Bioabsorbable Polymer Coating

November 29, 2012

News Conference News TCT 2012

Globalization of Innovation a ‘Must Have’ to Improve Health Care Delivery

October 22, 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

Boston Scientific Launches Victory Guidewire For Crossing Resistant Lesions In Peripheral Arteries

October 09, 2012

News Daily News

Endovascular Treatment of Stroke, Though Uncommon, Gains Ground

Caitlin E. Cox

September 18, 2012

News Industry News

Medtronic Launches Resolute Integrity Coronary Stent System in Japan

August 28, 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 Industry News

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

May 15, 2012

News Industry News

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

April 23, 2012

News Industry News

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

March 04, 2012

News Industry News

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

November 21, 2011

News Industry News

Boston Scientific Launches Promus Element™ Stent System In China

October 17, 2011

News Daily News

FDA, CMS Parallel Review Aims to Speed Access to Innovative Technologies

L.A. McKeown

October 14, 2011

News Daily News

Commentary Authors Urge Improvements to Device Approval Process

Caitlin E. Cox

July 20, 2011

News Industry News

First Edwards Transcatheter Valve Replacement Cases Performed in China

June 06, 2011

News Daily News

Many Cardiovascular Devices Approved by FDA Without Sex-Specific Data

L.A. McKeown

February 28, 2011

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Boston Scientific Concludes Enrollment In Randomized, Multicenter, Pivotal Study Of SYNERGY™ Coronary Stent System

Thoratec Acquires DuraHeart® II Ventricular Assist System

Edwards Lifesciences Comments on FDA Warning Letter

Boston Scientific Reports Lotus™ Valve System Met Primary Performance Endpoint in REPRISE II Trial

First Patient Enrolled in the Boston Scientific Multicenter Study of the SYNERGY™ Coronary Stent System Featuring a Bioabsorbable Polymer Coating

Globalization of Innovation a ‘Must Have’ to Improve Health Care Delivery

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

Boston Scientific Launches Victory Guidewire For Crossing Resistant Lesions In Peripheral Arteries

Endovascular Treatment of Stroke, Though Uncommon, Gains Ground

Medtronic Launches Resolute Integrity Coronary Stent System in Japan

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

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

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

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

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

Boston Scientific Launches Promus Element™ Stent System In China

FDA, CMS Parallel Review Aims to Speed Access to Innovative Technologies

Commentary Authors Urge Improvements to Device Approval Process

First Edwards Transcatheter Valve Replacement Cases Performed in China

Many Cardiovascular Devices Approved by FDA Without Sex-Specific Data

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