Atlas FDA

Edwards EVOQUE Transcatheter Tricuspid Valve Replacement System

FDA premarket approval P230013/S016 · decided 2025-08-13

Approval details

PMA number
P230013
Supplement
S016
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Edwards EVOQUE Transcatheter Tricuspid Valve Replacement System
Generic name
Percutaneously Delivered Prostheses and Tricuspid Valves
Applicant
Edwards Lifesciences, LLC
Date received
2025-06-17
Decision date
2025-08-13
Days to decision
57 days
Decision code
APPR
Product code
NPW
Advisory committee
Cardiovascular
Expedited review
No
Location
Irvine, CA
Statement
approval to add the Edwards Singapore facility, located in Changi, Singapore, as a qualified manufacturing site for the EVOQUE valve component of the EVOQUE TTVR System

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510(k) clearances by this applicant

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