FDA PMA FDA Class 3 30-Day Notice Accepted 🇺🇸 United States

Heart-Valve, Non-Allograft Tissue

PMA: P040021 · Supplement: S053 · Decision Oct 18, 2023
Classifications
1
FEI Numbers
19
Registration Numbers
19

Basic Information

Device Name
Heart-Valve, Non-Allograft Tissue
Trade Name
Epic™ Supra Valve, Epic™ Valve, Epic™ Plus Stented Tissue Valve, Epic™ Plus Supra Valve, Epic™ Max Valve
PMA Number
P040021
Supplement Number
S053
Device Class
FDA Class 3
Product Code
LWR
Generic Name
heart-valve, non-allograft tissue
Medical Specialty
Unknown
Advisory Committee
Cardiovascular
Decision
30-Day Notice Accepted
Decision Code
OK30
Decision Date
October 18, 2023
Date Received
September 19, 2023
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

A new sub-supplier for materials used in sutures

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