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EDWARDS PRIMA PLUS STENTLESS BIOPROSTHESIS, MODEL 2500P

FDA premarket approval P000007/S016 · decided 2008-05-22

Approval details

PMA number
P000007
Supplement
S016
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
EDWARDS PRIMA PLUS STENTLESS BIOPROSTHESIS, MODEL 2500P
Generic name
replacement Heart-valve
Applicant
Edwards Lifesciences, LLC
Date received
2008-05-08
Decision date
2008-05-22
Days to decision
14 days
Decision code
OK30
Product code
DYE
Advisory committee
Cardiovascular
Expedited review
No
Location
Irvine, CA
Statement
CHANGE IN SUPPLIERS FOR A POLYESTER RAW MATERIAL USED IN THE MANUFACTURE OF THE DEVICE.

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510(k) clearances by this applicant

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