FDA PMA FDA Class 3 Approved 🇺🇸 United States

Aortic Valve, Prosthesis, Percutaneously Delivered

PMA: P140031 · Supplement: S018 · Decision Nov 17, 2016
Classifications
1
FEI Numbers
24
Registration Numbers
24

Basic Information

Device Name
Aortic Valve, Prosthesis, Percutaneously Delivered
Trade Name
Commander Delivery System (Including Loader)
PMA Number
P140031
Supplement Number
S018
Device Class
FDA Class 3
Product Code
NPT
Generic Name
Aortic valve, prosthesis, percutaneously delivered
Medical Specialty
Unknown
Advisory Committee
Cardiovascular
Decision
Approved
Decision Code
APPR
Decision Date
November 17, 2016
Date Received
June 6, 2016
Supplement Type
Normal 180 Day Track No User Fee
Supplement Reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

Approval for the addition of the Draper, Utah manufacturing facility to manufacture the Commander Delivery System.

Classifications

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

Product Code Device Name
NPT Aortic Valve, Prosthesis, Percutaneously Delivered