| 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 | MEDTRONIC HALL PROSTHETIC HEART VALVE |
| Generic Name | HEART-VALVE, MECHANICAL |
| Applicant | Medtronic Cardiac Surgery 8299 Central Ave., NE Minneapolis, MN 55432 |
| PMA Number | P790018 |
| Supplement Number | S049 |
| Date Received | 08/11/2008 |
| Decision Date | 09/09/2008 |
| Withdrawal Date | 12/23/2011 |
| Product Code |
LWQ |
| Advisory Committee |
Cardiovascular |
| Supplement Type | 30-Day Notice |
| Supplement Reason | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
| Expedited Review Granted? | No |
| Combination Product | No |
| Predetermined Change Control Plan Authorized | No |
Approval Order Statement CHANGE IN VENDOR FOR A SUTURE USED IN THE MANUFACTURE OF THE DEVICES. |
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