| 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 | SYNVISC, SYNVISC-ONE |
| Generic Name | Acid, hyaluronic, intraarticular |
| Applicant | Sanofi Genzyme Corp. 450 Water St. Cambridge, MA 02141 |
| PMA Number | P940015 |
| Supplement Number | S033 |
| Date Received | 07/09/2014 |
| Decision Date | 08/21/2014 |
| Product Code |
MOZ |
| Advisory Committee |
Orthopedic |
| Supplement Type | Special (Immediate Track) |
| Supplement Reason | Labeling Change - Indications/instructions/shelf life/tradename |
| Expedited Review Granted? | No |
| Combination Product | No |
| Predetermined Change Control Plan Authorized | No |
| Recalls | CDRH Recalls |
Approval Order Statement APPROVAL FOR THE UPDATING OF THE PACKAGE INSERT AND PATIENT INFORMATION LEAFLET WITH RESPECT TO ADVERSE EVENT INFORMATION ON PSEUDOSEPSIS, ALLERGIC REACTIONS, AND HYPERSENSITIVITY. |
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