FDA PMA FDA Class 3 Approved 🇺🇸 United States

Replacement Heart-Valve

PMA: P980043 · Supplement: S056 · Decision Feb 7, 2017
Classifications
1
FEI Numbers
11
Registration Numbers
11

Basic Information

Device Name
Replacement Heart-Valve
Trade Name
HANCOCK II PORCINE BIOPROSTHESIS
PMA Number
P980043
Supplement Number
S056
Device Class
FDA Class 3
Product Code
DYE
Generic Name
replacement Heart-valve
Regulation Number
870.3925
Medical Specialty
Cardiovascular
Advisory Committee
Cardiovascular
Decision
Approved
Decision Code
APPR
Decision Date
February 7, 2017
Date Received
November 10, 2016
Supplement Type
Real-Time Process
Supplement Reason
Labeling Change - Indications/instructions/shelf life/tradename
Expedited Review
N

Advisory Committee Statement

Approval for changes to the labeling content and format for the Mosaic, Hancock II, and Freestyle Bioprostheses.

Classifications

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

Product Code Device Name
DYE Replacement Heart-Valve