Atlas FDA

Edwards EVOQUE Tricuspid Valve Replacement System

FDA premarket approval P230013/S009 · decided 2024-08-30

Approval details

PMA number
P230013
Supplement
S009
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Edwards EVOQUE Tricuspid Valve Replacement System
Generic name
Percutaneously Delivered Prostheses and Tricuspid Valves
Applicant
Edwards Lifesciences, LLC
Date received
2024-08-06
Decision date
2024-08-30
Days to decision
24 days
Decision code
OK30
Product code
NPW
Advisory committee
Cardiovascular
Expedited review
No
Location
Irvine, CA
Statement
an alternative in-house supplier for the lumen subassemblies of the EVOQUE delivery system

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510(k) clearances by this applicant

RecordFirmDate
Respiration Rate algorithm (K251326)Edwards Lifesciences, LLC2026-06-11
HemoSphere Nano Monitor (HSNANO1) (K253186)Edwards Lifesciences, LLC2026-02-24
Edwards MC3 Tricuspid annuloplasty ring (4900) (K251982)Edwards Lifesciences, LLC2025-09-23
Carpentier-Edwards Physio Annuloplasty Ring (4450) (K251688)Edwards Lifesciences, LLC2025-09-17
Hypertension Prediction Index (HePI) Algorithm (K242518)Edwards Lifesciences, LLC2025-05-15
FloTrac sensors; FloTrac Jr sensors; Acumen IQ sensors; VolumeView sensors (K242909)Edwards Lifesciences, LLC2025-03-21
Fogarty Thru-Lumen Embolectomy Catheter (K240078)Edwards Lifesciences, LLC2024-08-28
Acumen Assisted Fluid Management (AFM) Software Feature (K233984)Edwards Lifesciences, LLC2024-08-02