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 | Zenith Fenestrated AAA Endovascular Graft |
Generic Name | SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT |
Applicant | COOK, INC. 750 Daniels Way P.O. Box 489 Bloomington, IN 47402 |
PMA Number | P020018 |
Supplement Number | S063 |
Date Received | 04/05/2024 |
Decision Date | 04/29/2024 |
Product Code |
MIH |
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 use of an alternative suture in manufacturing of the Zenith® Fenestrated AAA Endovascular Graft, Zenith Alpha™ Thoracic Endovascular Graft, and Zenith® Dissection Endovascular System |
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