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Expert Consensus Document on TAVR Provides ‘Roadmap’ for Clinicians

Yael L. Maxwell

March 06, 2012

News Industry News

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

February 29, 2012

News Daily News

Live Case Procedures Just as Safe as in Daily Practice

Caitlin E. Cox

February 21, 2012

News Industry News

Boston Scientific Launches Innovative Crossing Device to Treat Complete Blockages in Peripheral Arteries

February 07, 2012

News Industry News

Vascular Solutions Launches Reprocessing Service for Closurefast® Vein Catheters

January 31, 2012

News Industry News

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

November 21, 2011

News Industry News

FDA Approves XARELTO® (rivaroxaban) to Reduce the Risk of Stroke and Systemic Embolism in Patients with Nonvalvular Atrial Fibrillation

November 04, 2011

News Daily News

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

L.A. McKeown

October 14, 2011

News Daily News

NEJM Articles Argue to Sack FDA’s Device Clearance Process

Caitlin E. Cox

August 12, 2011

News Daily News

FDA Panel Recommends Approval of Transcatheter Heart Valve

July 21, 2011

News Industry News

PLC Ramps Up for U.S. Clinical Trial of RenalGuard®

June 02, 2011

News Industry News

InfraReDx Receives CE Mark Approval In EU For LipiScan IVUS Coronary Imaging System

April 21, 2011

News Industry News

Boston Scientific Announces European Approval and Launch of OMEGA™ Platinum Chromium Stent System

March 06, 2011

News Daily News

Many Cardiovascular Devices Approved by FDA Without Sex-Specific Data

L.A. McKeown

February 28, 2011

News Daily News

Report on Device Recalls Criticizes Current FDA Approval Process

L.A. McKeown

February 14, 2011

News Daily News

Parsing the Panel: Reactions to Expanding CAS to Standard-Risk Patients

Caitlin E. Cox

January 27, 2011

News Industry News

Boston Scientific to Acquire Atritech

January 18, 2011

News Industry News

Bayer’s Rivaroxaban Submitted for Marketing Authorisation in Stroke Prevention in Patients with Atrial Fibrillation in the US

January 04, 2011

News Industry News

Bayer’s Rivaroxaban Submitted for EU Marketing Authorisation in Stroke Prevention in Patients with Atrial Fibrillation as well as for the Treatment of Deep Vein Thrombosis

January 04, 2011

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Expert Consensus Document on TAVR Provides ‘Roadmap’ for Clinicians

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

Live Case Procedures Just as Safe as in Daily Practice

Boston Scientific Launches Innovative Crossing Device to Treat Complete Blockages in Peripheral Arteries

Vascular Solutions Launches Reprocessing Service for Closurefast® Vein Catheters

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

FDA Approves XARELTO® (rivaroxaban) to Reduce the Risk of Stroke and Systemic Embolism in Patients with Nonvalvular Atrial Fibrillation

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

NEJM Articles Argue to Sack FDA’s Device Clearance Process

FDA Panel Recommends Approval of Transcatheter Heart Valve

PLC Ramps Up for U.S. Clinical Trial of RenalGuard®

InfraReDx Receives CE Mark Approval In EU For LipiScan IVUS Coronary Imaging System

Boston Scientific Announces European Approval and Launch of OMEGA™ Platinum Chromium Stent System

Many Cardiovascular Devices Approved by FDA Without Sex-Specific Data

Report on Device Recalls Criticizes Current FDA Approval Process

Parsing the Panel: Reactions to Expanding CAS to Standard-Risk Patients

Boston Scientific to Acquire Atritech

Bayer’s Rivaroxaban Submitted for Marketing Authorisation in Stroke Prevention in Patients with Atrial Fibrillation in the US

Bayer’s Rivaroxaban Submitted for EU Marketing Authorisation in Stroke Prevention in Patients with Atrial Fibrillation as well as for the Treatment of Deep Vein Thrombosis

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