Atlas FDA

Crimper

FDA premarket approval P200015/S062 · decided 2025-03-25

Approval details

PMA number
P200015
Supplement
S062
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Crimper
Generic name
Pulmonary valve prosthesis percutaneously delivered
Applicant
Edwards Lifesciences, LLC
Date received
2025-02-24
Decision date
2025-03-25
Days to decision
29 days
Decision code
OK30
Product code
NPV
Advisory committee
Cardiovascular
Expedited review
No
Location
Irvine, CA
Statement
an alternative sampling plan for pyrogen testing of the Crimper component

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