Atlas FDA

Injection Molding Crimper 9600CR Components

FDA premarket approval P200015/S056 · decided 2024-08-12

Approval details

PMA number
P200015
Supplement
S056
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Injection Molding Crimper 9600CR Components
Generic name
Pulmonary valve prosthesis percutaneously delivered
Applicant
Edwards Lifesciences, LLC
Date received
2024-07-29
Decision date
2024-08-12
Days to decision
14 days
Decision code
OK30
Product code
NPV
Advisory committee
Cardiovascular
Expedited review
No
Location
Irvine, CA
Statement
implementing in-house injection molding of crimper components

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510(k) clearances by this applicant

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