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CARPENTIER-EDWARDS PERIMOUNT PERICARDIAL BIOPROSTHESIS MODELS

FDA premarket approval P860057/S062 · decided 2010-01-05

Approval details

PMA number
P860057
Supplement
S062
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
CARPENTIER-EDWARDS PERIMOUNT PERICARDIAL BIOPROSTHESIS MODELS
Generic name
replacement Heart-valve
Applicant
Edwards Lifesciences, LLC
Date received
2009-11-06
Decision date
2010-01-05
Days to decision
60 days
Decision code
APPR
Product code
DYE
Advisory committee
Cardiovascular
Expedited review
No
Location
Irvine, CA
Statement
APPROVAL FOR ELIMINATION OF STENT CREEP TESTING FROM THE SHELF LIFE TESTING PROTOCOL FOR THE PERIMOUNT BIOPROSTHETIC VALVES TREATED WITH THE THERMAFIX PROCESS.

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