Note: This medical device record is a PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information. |
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Device | EDWARDS SAPIEN TRANSCATHETER HEART VALVE |
Generic Name | aortic valve, prosthesis, percutaneously delivered |
Applicant | EDWARDS LIFESCIENCES, LLC. one edwards way irvine, CA 92614 |
PMA Number | P100041 |
Supplement Number | S038 |
Date Received | 08/20/2013 |
Decision Date | 09/20/2013 |
Withdrawal Date
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03/18/2019 |
Product Code |
NPT |
Advisory Committee |
Cardiovascular |
Supplement Type | 30-day notice |
Supplement Reason | process change - manufacturer/sterilizer/packager/supplier |
Expedited Review Granted? | No |
Combination Product | No |
Approval Order Statement UPDATE TO THE TISSUE FIXATION SYSTEM USING A NEW AUTOMATED PROCESS. |
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