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Displaying 1 - 20 of 20
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FDA Expands Evolut Indication to Include Redo TAVI
News Daily News

FDA Expands Evolut Indications to Include Redo TAVI

Yael L. Maxwell
Yael L. Maxwell
August 29, 2025
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
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
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
FDA Approves Portico TAVI Valve, Paving the Way for Third US Device
News Daily News

FDA Approves Portico TAVI Valve, Paving the Way for Third US Device

Shelley Wood
Shelley Wood
September 20, 2021
Sapien 3 Valve Approved in Europe for Low-Risk Patients
News Daily News

Sapien 3 Valve Approved in Europe for Low-Risk Patients

Michael O'Riordan
Michael O'Riordan
November 06, 2019
FDA Expands TAVR Indication to Low-Risk Patients
News Daily News

FDA Expands TAVR Indication to Low-Risk Patients

Michael O'Riordan
Michael O'Riordan
August 16, 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 Clears Next-Generation Sapien 3 Ultra TAVR Valve
News Daily News

FDA Clears Next-Generation Sapien 3 Ultra TAVR Valve

Todd Neale
Todd Neale
January 02, 2019
FDA Approves Rivaroxaban for CV Event Reduction in CAD and PAD Patients
News Daily News

FDA Approves Rivaroxaban for CV Event Reduction in CAD and PAD Patients

Todd Neale
Todd Neale
October 12, 2018
‘The Bleeding Edge’ Documentary, Tackling Medical Device Regulation, Spurs Diverse Cardiology Reactions
News Daily News

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

Yael L. Maxwell
Yael L. Maxwell
August 17, 2018
LV Diastolic Dysfunction Linked With Higher Mortality Post-TAVR
News Daily News

LV Diastolic Dysfunction Linked With Higher Mortality Post-TAVR

Yael L. Maxwell
Yael L. Maxwell
March 01, 2018
FDA Expands CoreValve Indication to Include Intermediate-Risk Patients
News Daily News

FDA Expands CoreValve Indication to Include Intermediate-Risk Patients

Michael O'Riordan
Michael O'Riordan
July 10, 2017
FDA Clears Sentinel Cerebral Protection Device for Use During TAVR
News Daily News

FDA Clears Sentinel Cerebral Protection Device for Use During TAVR

Shelley Wood
Shelley Wood
June 05, 2017
News Daily News

FDA Approves Next-Gen CoreValve Evolut PRO Valve

Todd Neale
Todd Neale
March 22, 2017
News Daily News

FDA Approves 34-mm TAVR Valve for Patients With Larger Anatomy

L.A. McKeown
L.A. McKeown
October 27, 2016
News Daily News

Sapien 3 Approved for Use in Intermediate-Risk Patients in Europe

Michael O'Riordan
Michael O'Riordan
September 20, 2016
News Daily News

TAVR as an Option for Intermediate-Risk Patients: Physicians Respond

Yael L. Maxwell
Yael L. Maxwell
August 24, 2016
News Daily News

FDA Approves Sapien XT and Sapien 3 for Intermediate-Risk Patients

Yael L. Maxwell
Yael L. Maxwell
August 18, 2016
News Daily News

Next-Generation CoreValve Device Receives CE Mark for Use in Intermediate-Risk Patients

Todd Neale
Todd Neale
August 01, 2016
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