| 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 | Biocor™, Biocor™ Supra, Epic™, Epic™ Supra, Epic™ Plus, Epic™ Plus Supra |
| Generic Name | heart-valve, non-allograft tissue |
| Applicant | ABBOTT MEDICAL 177 County Rd. B E. St. Paul, MN 55117 |
| PMA Number | P040021 |
| Supplement Number | S048 |
| Date Received | 11/08/2021 |
| Decision Date | 12/16/2021 |
| Product Code |
LWR |
| 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 Discontinuation of passive monitoring procedures in ISO Class 7 and 8 cleanrooms. |
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