FDA PMA FDA Class 3 Approved 🇺🇸 United States

Heart-Valve, Non-Allograft Tissue

PMA: P150048 · Supplement: S047 · Decision Mar 16, 2022
Classifications
1
FEI Numbers
19
Registration Numbers
19

Basic Information

Device Name
Heart-Valve, Non-Allograft Tissue
Trade Name
MITRIS RESILIA Mitral Valve
PMA Number
P150048
Supplement Number
S047
Device Class
FDA Class 3
Product Code
LWR
Generic Name
heart-valve, non-allograft tissue
Medical Specialty
Unknown
Advisory Committee
Cardiovascular
Decision
Approved
Decision Code
APPR
Decision Date
March 16, 2022
Date Received
August 3, 2020
Supplement Type
Normal 180 Day Track
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

Approval for material and design modifications related to the wireform, sewing ring, valve holder and valve handle

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LWR Heart-Valve, Non-Allograft Tissue