FDA PMA FDA Class 3 Approved 🇺🇸 United States

Heart-Valve, Mechanical

PMA: P990046 · Supplement: S050 · Decision Dec 13, 2017
Classifications
1
FEI Numbers
17
Registration Numbers
17

Basic Information

Device Name
Heart-Valve, Mechanical
Trade Name
Open Pivot Heart Valve / Aortic Valved Graft
PMA Number
P990046
Supplement Number
S050
Device Class
FDA Class 3
Product Code
LWQ
Generic Name
HEART-VALVE, MECHANICAL
Medical Specialty
Unknown
Advisory Committee
Cardiovascular
Decision
Approved
Decision Code
APPR
Decision Date
December 13, 2017
Date Received
August 14, 2017
Supplement Type
135 Review Track For 30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

Approval for a transfer of manufacturing operations to a new controlled environment area within the same manufacturing site.

Classifications

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

Product Code Device Name
LWQ Heart-Valve, Mechanical