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Class I Recall for Amplatzer LAAO's Steerable Delivery Sheath

Shelley Wood

July 26, 2023

News Daily News

Penumbra’s JET 7 Recall: A Kick Start to Change?

Caitlin E. Cox

December 01, 2021

News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for April 2021

Caitlin E. Cox

May 03, 2021

News Daily News

FDA: Penumbra JET 7 Clot Retrievers Recalled Following Deaths, Injuries

Shelley Wood

December 16, 2020

News Daily News

TCTMD’s Top 10 Most Popular Stories for April 2019

Shelley Wood

May 01, 2019

News Daily News

Sentinel Cerebral Embolic Protection Device Acquired by Boston Scientific

Shelley Wood

July 20, 2018

News Daily News

Penumbra Stent Retriever Recalled Due to Potential for Wire to Break, Separate

Todd Neale

July 21, 2017

News Daily News

TCTMD’s Top 10 Most Popular Stories for June 2017

Shelley Wood

July 03, 2017

News Daily News

FDA: ROCKET AF Results Not Affected by Faulty INR Testing in Warfarin Arm

Michael O'Riordan

October 11, 2016

Cerebral Protection in TAVR: New Insights, New Questions as First Device Seeks FDA Clearance

Shelley Wood

September 22, 2016

News Daily News

FDA: Vascu-Guard Patch Associated With Bleeding, Death After Carotid Endarterectomy

Yael L. Maxwell

September 02, 2016

News Daily News

FDA Tackles Regulatory, Scientific Issues With Point-of-Care Coagulation Monitoring Devices

Todd Neale

March 24, 2016

News Daily News

ROCKET AF Investigators: Problems With Warfarin Monitoring Device Did Not Skew Results

Todd Neale

February 04, 2016

News Daily News

FDA Sounds Alarm Bells Over Use of Lariat Device for LAA Closure in A-fib Patients

Yael L. Maxwell

July 17, 2015

News Daily News

Commentary Authors Urge Improvements to Device Approval Process

Caitlin E. Cox

July 20, 2011

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Class I Recall for Amplatzer LAAO's Steerable Delivery Sheath

Penumbra’s JET 7 Recall: A Kick Start to Change?

TCTMD’s Top 10 Most Popular Stories for April 2021

FDA: Penumbra JET 7 Clot Retrievers Recalled Following Deaths, Injuries

TCTMD’s Top 10 Most Popular Stories for April 2019

Sentinel Cerebral Embolic Protection Device Acquired by Boston Scientific

Penumbra Stent Retriever Recalled Due to Potential for Wire to Break, Separate

TCTMD’s Top 10 Most Popular Stories for June 2017

FDA: ROCKET AF Results Not Affected by Faulty INR Testing in Warfarin Arm

Cerebral Protection in TAVR: New Insights, New Questions as First Device Seeks FDA Clearance

FDA: Vascu-Guard Patch Associated With Bleeding, Death After Carotid Endarterectomy

FDA Tackles Regulatory, Scientific Issues With Point-of-Care Coagulation Monitoring Devices

ROCKET AF Investigators: Problems With Warfarin Monitoring Device Did Not Skew Results

FDA Sounds Alarm Bells Over Use of Lariat Device for LAA Closure in A-fib Patients

Commentary Authors Urge Improvements to Device Approval Process

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