Atlas FDA

EDWARDS SAPIEN TRANSCATHETER HEART VALVE

FDA premarket approval P100041/S011 · decided 2012-11-06

Approval details

PMA number
P100041
Supplement
S011
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Postapproval Study Protocol - OSB
Trade name
EDWARDS SAPIEN TRANSCATHETER HEART VALVE
Generic name
Aortic valve, prosthesis, percutaneously delivered
Applicant
Edwards Lifesciences, LLC
Date received
2012-06-08
Decision date
2012-11-06
Days to decision
151 days
Decision code
APPR
Product code
NPT
Advisory committee
Cardiovascular
Expedited review
No
Location
Irvine, CA
Statement
APPROVAL OF THE POST-APPROVAL STUDY PROTOCOL.

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