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 | HYMOVIS® |
Generic Name | Acid, hyaluronic, intraarticular |
Applicant | FIDIA FARMACEUTICI PONTE DELLA FABBRICA 3/A ABANO TERME 35031 |
PMA Number | P150010 |
Supplement Number | S002 |
Date Received | 07/11/2022 |
Decision Date | 08/08/2022 |
Product Code |
MOZ |
Advisory Committee |
Orthopedic |
Supplement Type | 30-Day Notice |
Supplement Reason | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
Expedited Review Granted? | No |
Combination Product | No |
Approval Order Statement Change from manual to automated syringe quality inspection. |
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