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Carpentier-Edwards PERIMOUNT Pericardial Aortic Bioprosthesis; Theon Pericardial Aortic Bioprosthesis with ThermaFix tis

FDA premarket approval P860057/S171 · decided 2017-12-08

Approval details

PMA number
P860057
Supplement
S171
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Carpentier-Edwards PERIMOUNT Pericardial Aortic Bioprosthesis; Theon Pericardial Aortic Bioprosthesis with ThermaFix tis
Generic name
replacement Heart-valve
Applicant
Edwards Lifesciences, LLC
Date received
2017-11-09
Decision date
2017-12-08
Days to decision
29 days
Decision code
OK30
Product code
DYE
Advisory committee
Cardiovascular
Expedited review
No
Location
Irvine, CA
Statement
Addition of new manufacturing equipment to an existing cleanroom.

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