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CARPENTIER-EDWARDS PERIMOUNT AORTIC & MITRAL BIOPROSTHESIS FAMILIES

FDA premarket approval P860057/S135 · decided 2015-06-11

Approval details

PMA number
P860057
Supplement
S135
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
CARPENTIER-EDWARDS PERIMOUNT AORTIC & MITRAL BIOPROSTHESIS FAMILIES
Generic name
replacement Heart-valve
Applicant
Edwards Lifesciences, LLC
Date received
2015-03-23
Decision date
2015-06-11
Days to decision
80 days
Decision code
APPR
Product code
DYE
Advisory committee
Cardiovascular
Expedited review
No
Location
Irvine, CA
Statement
APPROVAL FOR MODIFICATION (ELIMINATION) TO THE CENTRAIL-HOLE-IN-AIR SPECIFICATION.

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