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EDWARDS SAPIEN XT TRANSCATHETER HEART VALVE AND ACCESSORIES

FDA premarket approval P130009/S060 · decided 2016-06-27

Approval details

PMA number
P130009
Supplement
S060
Supplement type
Special (Immediate Track)
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
EDWARDS SAPIEN XT TRANSCATHETER HEART VALVE AND ACCESSORIES
Generic name
Aortic valve, prosthesis, percutaneously delivered
Applicant
Edwards Lifesciences, LLC
Date received
2016-06-02
Decision date
2016-06-27
Days to decision
25 days
Decision code
APPR
Product code
NPT
Advisory committee
Cardiovascular
Expedited review
No
Location
Irvine, CA
Statement
Approval for the addition of a new inspection step to the final inspection process for the Edwards Expandable Introducer Sheath Set.

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510(k) clearances by this applicant

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