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Displaying 1 - 20 of 20
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FDA Approves TAVI for Asymptomatic Patients With Severe Aortic Stenosis
News Daily News

FDA Approves TAVI for Asymptomatic Patients With Severe Aortic Stenosis

Michael O'Riordan
Michael O'Riordan
May 01, 2025
FDA Approves Bioresorbable Scaffold for BTK Lesions
News Daily News

FDA Approves Bioresorbable Scaffold for BTK Lesions

Michael O'Riordan
Michael O'Riordan
April 29, 2024
Biologic Winrevair Wins FDA Approval for Treatment of PAH
News Daily News

Biologic Winrevair Wins FDA Approval for Treatment of PAH

L.A. McKeown
L.A. McKeown
March 27, 2024
Mechanism’s Mojo ‘Obvious’ CV Therapies More Likely to Be Seen as Effective
News Daily News

Mechanism’s Mojo: ‘Obvious’ CV Therapies More Likely to Be Seen as Effective

Michael O'Riordan
Michael O'Riordan
February 23, 2024
FDA Approves Blood Flow-Diverting LimFlow System for No-Option CLTI
News Daily News

FDA Approves Blood Flow-Diverting LimFlow System for No-Option CLTI

L.A. McKeown
L.A. McKeown
September 12, 2023
Aveir DR Dual-Chamber Leadless Pacemaker Wins FDA Approval
News Daily News

Aveir DR Dual-Chamber Leadless Pacemaker Wins FDA Approval

L.A. McKeown
L.A. McKeown
July 06, 2023
Medical Devices Cleared on Faulty Predicates More Likely to be Recalled
News Daily News

Medical Devices Cleared on Faulty Predicates More Likely to be Recalled

Michael O'Riordan
Michael O'Riordan
January 17, 2023
Higher Annual TAVI Volumes Linked to Greater Use of Embolic Protection
News Daily News

Higher Annual TAVI Volumes Linked to Greater Use of Embolic Protection

L.A. McKeown
L.A. McKeown
August 23, 2022
Postmarketing Studies of CV Devices Still Lacking in the US
News Daily News

Postmarketing Studies of CV Devices Still Lacking in the US

Caitlin E. Cox
Caitlin E. Cox
March 17, 2022
Add-on CMS Payment Sweetens Shockwave Choice, but Cost Still Rankles
News Daily News

Add-on CMS Payment Sweetens Shockwave Choice, but Cost Still Rankles

Michael O'Riordan
Michael O'Riordan
May 12, 2021
Xience Cleared in Europe for 1-Month DAPT in High-Bleeding-Risk Patients
News Daily News

Xience Cleared in Europe for 1-Month DAPT in High-Bleeding-Risk Patients

Shelley Wood
Shelley Wood
April 06, 2021
FDA Advisors Unconvinced by Lutonix BTK Drug-Coated Balloon
News Daily News

FDA Advisors Unconvinced by Lutonix BTK Drug-Coated Balloon

L.A. McKeown
L.A. McKeown
February 18, 2021
FDA Extends Ticagrelor Indication to High-Risk CAD Primary Prevention
News Daily News

FDA Extends Ticagrelor Indication to High-Risk CAD Primary Prevention

Shelley Wood
Shelley Wood
June 01, 2020
TCTMD’s Top 10 Most Popular Stories for August 2019
News Daily News

TCTMD’s Top 10 Most Popular Stories for August 2019

Shelley Wood
Shelley Wood
August 30, 2019
FDA Grants Cardiac MR Indication for Gadavist Contrast Injection
News Daily News

FDA Grants Cardiac MR Indication for Gadavist Contrast Injection

Shelley Wood
Shelley Wood
July 16, 2019
TCTMD’s Top 10 Most Popular Stories for April 2019
News Daily News

TCTMD’s Top 10 Most Popular Stories for April 2019

Shelley Wood
Shelley Wood
May 01, 2019
FDA Approves Lotus Edge, Ushering Third Device Into US Market
News Daily News

FDA Approves Lotus Edge, Ushering Third Device Into US Market

Shelley Wood
Shelley Wood
April 24, 2019
FDA Grants Approval to TherOx for Supersaturated Oxygen Therapy in LAD STEMI
News Daily News

FDA Grants Approval to TherOx for Supersaturated Oxygen Therapy in LAD STEMI

L.A. McKeown
L.A. McKeown
April 04, 2019
FDA Extends MitraClip Indication to Include Functional MR
News Daily News

FDA Extends MitraClip Indication to Include Functional MR

Shelley Wood
Shelley Wood
March 14, 2019
FDA Approves Pea-Sized Occluder for Patent Ductus Arteriosus in Premature Babies
News Daily News

FDA Approves Pea-Sized Occluder for Patent Ductus Arteriosus in Premature Babies

L.A. McKeown
L.A. McKeown
January 14, 2019
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