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FDA Issues Early Alert About Risks of Peripheral Atherectomy Device

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FDA Issues Early Alert About Risks of Peripheral Atherectomy Device

February 07, 2025

FDA: All Restrictions on Paclitaxel Devices for PAD Are Removed

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FDA: All Restrictions on Paclitaxel Devices for PAD Are Removed

July 11, 2023

Medtronic Recalls TurboHawk Plus Atherectomy System

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Medtronic Recalls TurboHawk Plus Atherectomy System

March 09, 2022

HawkOne Directional Atherectomy System Recalled Due to Risk of Tip Breakage

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HawkOne Directional Atherectomy System Recalled Due to Risk of Tip Breakage

January 21, 2022

FDA Class I Recall for PTA Catheters Due to Unexpected Balloon Bursting

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FDA Class I Recall for PTA Catheters Due to Unexpected Balloon Bursting

Yael L. Maxwell

June 18, 2019

TCTMD’s Top 10 Most Popular Stories for May 2019

News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for May 2019

May 31, 2019

FDA Analysis Points to Higher Death Risk With Paclitaxel-Based Devices for PAD

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FDA Analysis Points to Higher Death Risk With Paclitaxel-Based Devices for PAD

March 15, 2019

Mortality Data ‘Inadvertently Omitted’ From IN.PACT Analysis of Paclitaxel-Coated Balloons

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Mortality Data ‘Inadvertently Omitted’ From IN.PACT Analysis of Paclitaxel-Coated Balloons

February 19, 2019

TCTMD’s Top 10 Most Popular Stories for January 2019

News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for January 2019

January 31, 2019

Paclitaxel in PAD: What to Tell Patients While the Numbers Are Crunched

News Conference News ISET 2019

Paclitaxel in PAD: What to Tell Patients While the Numbers Are Crunched

January 28, 2019

News Daily News

Wingman35 Crossing Catheters Recalled Due to Tip Splitting, Separation

May 04, 2017

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