FDA PMA FDA Class 3 Approved 🇺🇸 United States

Replacement Heart-Valve

PMA: P990064 · Supplement: S015 · Decision Aug 25, 2006
Classifications
1
FEI Numbers
11
Registration Numbers
11

Basic Information

Device Name
Replacement Heart-Valve
Trade Name
MOSAIC PORCINE BIOPROSTHESIS
PMA Number
P990064
Supplement Number
S015
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
August 25, 2006
Date Received
April 17, 2006
Supplement Type
Normal 180 Day Track No User Fee
Supplement Reason
Labeling Change - Indications/instructions/shelf life/tradename
Expedited Review
N

Advisory Committee Statement

APPROVAL FOR CHANGES TO THE INSTRUCTIONS FOR USE (IFU) BASED ON THE RESULTS OF THE COMPLETED POST-MARKET STUDY OF THE DEVICE.

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