| 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 | APLIGRAF |
| Generic Name | Dressing, wound and burn, interactive |
| Applicant | Organogenesis, Inc. 150 Dan Rd. Canton, MA 02021 |
| PMA Number | P950032 |
| Supplement Number | S069 |
| Date Received | 10/31/2012 |
| Decision Date | 11/20/2012 |
| Conversion Date | 08/14/2013 |
| Product Code |
MGR |
| Advisory Committee |
General & Plastic Surgery |
| Supplement Type | Real-Time Process |
| Supplement Reason | Change Design/Components/Specifications/Material |
| Expedited Review Granted? | No |
| Combination Product | Yes |
| Predetermined Change Control Plan Authorized | No |
| Recalls | CDRH Recalls |
Approval Order Statement APPROVAL FOR THE INTRODUCTION OF HUMAN EPIDERMAL KERATINOCYTE CELL STRAIN 200 (HEP 200) INTO THE MANUFACTURE OF THE DEVICE. |
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