Search - tctmd.com

Displaying 1 - 18 of 18

Sort: Relevancy | Date

News Daily News

‘Sobering’ Adverse Event Rate With Evoque Seen in Real-world Use

Yael L. Maxwell

June 18, 2025

News Daily News

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

Caitlin E. Cox

December 01, 2021

News Daily News

VASCADE Closure Device: FDA Database Tracks Common Complications, Deaths

Caitlin E. Cox

September 10, 2021

News Daily News

No Harm, No Help With Bioabsorbable-Polymer Stents: Registry

Michael O'Riordan

March 01, 2021

News Daily News

FDA Data Raise Red Flags for Suture-Based Vascular Closure Devices

Caitlin E. Cox

February 11, 2021

News Daily News

No Volume-Outcome Link With Watchman for LAA Closure? Single-Center Study

Michael O'Riordan

August 19, 2019

News Daily News

More Acute Stent Thrombosis With Synergy Stent in Bern PCI Registry

Michael O'Riordan

August 14, 2019

News Daily News

CV Devices in the Fast Lane: FDA’s Approval Often Rests on Early Evidence

Caitlin E. Cox

September 05, 2018

News Daily News

‘The Bleeding Edge’ Documentary, Tackling Medical Device Regulation, Spurs Diverse Cardiology Reactions

Yael L. Maxwell

August 17, 2018

News Daily News

Complications Spiked, Then Fell, After Initial Introduction of Watchman LAA Closure Device

Todd Neale

October 12, 2017

News Daily News

Pulmonary Artery Injury More Likely With Real-World Use of CardioMEMS, Analysis Suggests

Todd Neale

September 19, 2017

News Daily News

FDA Warns of Class I Recall of Chariot Guiding Sheath Used in Peripheral Procedures

Shelley Wood

December 10, 2015

News Daily News

La FDA Da la Voz de Alarma sobre el Uso del Dispositivo Lariat para el Cierre del AAI en Pacientes con FA

Yael L. Maxwell

July 17, 2015

News Daily News

FDA对在房颤患者中使用Lariat左心耳封堵装置发出警示

Yael L. Maxwell

July 17, 2015

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

一项研究调查了采用Lariat装置施行LAA封堵的并发症

May 05, 2015

News Daily News

Un Estudio Documenta las Complicaciones del Cierre del AAI con el Dispositivo Lariat

May 05, 2015

News Daily News

Study Documents Complications of LAA Closure With the Lariat Device

May 05, 2015

Advertisement

‘Sobering’ Adverse Event Rate With Evoque Seen in Real-world Use

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

VASCADE Closure Device: FDA Database Tracks Common Complications, Deaths

No Harm, No Help With Bioabsorbable-Polymer Stents: Registry

FDA Data Raise Red Flags for Suture-Based Vascular Closure Devices

No Volume-Outcome Link With Watchman for LAA Closure? Single-Center Study

More Acute Stent Thrombosis With Synergy Stent in Bern PCI Registry

CV Devices in the Fast Lane: FDA’s Approval Often Rests on Early Evidence

‘The Bleeding Edge’ Documentary, Tackling Medical Device Regulation, Spurs Diverse Cardiology Reactions

Complications Spiked, Then Fell, After Initial Introduction of Watchman LAA Closure Device

Pulmonary Artery Injury More Likely With Real-World Use of CardioMEMS, Analysis Suggests

FDA Warns of Class I Recall of Chariot Guiding Sheath Used in Peripheral Procedures

La FDA Da la Voz de Alarma sobre el Uso del Dispositivo Lariat para el Cierre del AAI en Pacientes con FA

FDA对在房颤患者中使用Lariat左心耳封堵装置发出警示

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

一项研究调查了采用Lariat装置施行LAA封堵的并发症

Un Estudio Documenta las Complicaciones del Cierre del AAI con el Dispositivo Lariat

Study Documents Complications of LAA Closure With the Lariat Device

Advertisement

Advertisement

Sign In

Forgot Your Password?

Search TCTMD

CME TITLE

Sign up for our newsletter

Search TCTMD

Submit an Event

Become a PREMIUM MEMBER or LOG IN to view exclusive content

REGISTER for free or LOG IN to view this content