Atlas FDA

Edwards Crimper 9600CR

FDA premarket approval P140031/S163 · decided 2023-08-25

Approval details

PMA number
P140031
Supplement
S163
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Edwards Crimper 9600CR
Generic name
Aortic valve, prosthesis, percutaneously delivered
Applicant
Edwards Lifesciences, LLC
Date received
2023-08-11
Decision date
2023-08-25
Days to decision
14 days
Decision code
OK30
Product code
NPT
Advisory committee
Cardiovascular
Expedited review
No
Location
Irvine, CA
Statement
Add a receiving inspection at the Edwards Añasco, Puerto Rico facility to support the manufacturing line for the Crimper.

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510(k) clearances by this applicant

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Respiration Rate algorithm (K251326)Edwards Lifesciences, LLC2026-06-11
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