Atlas FDA

Edwards SAPIEN 3 Transcatheter Heart Valves

FDA premarket approval P140031/S068 · decided 2018-07-11

Approval details

PMA number
P140031
Supplement
S068
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Edwards SAPIEN 3 Transcatheter Heart Valves
Generic name
Aortic valve, prosthesis, percutaneously delivered
Applicant
Edwards Lifesciences, LLC
Date received
2018-06-28
Decision date
2018-07-11
Days to decision
13 days
Decision code
OK30
Product code
NPT
Advisory committee
Cardiovascular
Expedited review
No
Location
Irvine, CA
Statement
Addition of a verification step during final valve packaging.

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510(k) clearances by this applicant

RecordFirmDate
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Carpentier-Edwards Physio Annuloplasty Ring (4450) (K251688)Edwards Lifesciences, LLC2025-09-17
Hypertension Prediction Index (HePI) Algorithm (K242518)Edwards Lifesciences, LLC2025-05-15
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