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

Heart-Valve, Non-Allograft Tissue

PMA: P150036 · Supplement: S055 · Decision Aug 31, 2021
Classifications
1
FEI Numbers
19
Registration Numbers
19

Basic Information

Device Name
Heart-Valve, Non-Allograft Tissue
Trade Name
EDWARDS INTUITY Elite™ Aortic Valve
PMA Number
P150036
Supplement Number
S055
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
August 31, 2021
Date Received
August 2, 2021
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

Ttransfer of downstream manufacturing processes for the EDWARDS INTUITY Elite Valve (Model 8300AB) to another established facility.

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