Medical Device Recalls
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11 to 13 of 13 Results
510(K) Number: K962152 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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SCORPIO TOTAL KNEE MEDIALIZED DOME PATELLA-SZ #5 -Intended for knee replacement Part Number:... | 2 | 01/31/2024 | Howmedica Osteonics Corp. |
SCORPIO TOTAL KNEE CONCENTRIC DOME PATELLA-SZ #9 -Intended for knee replacement Part Number:... | 2 | 01/31/2024 | Howmedica Osteonics Corp. |
SCORPIO TOTAL KNEE MEDIALIZED DOME PATELLA-SZ #11 -Intended for knee replacement Part Numbe... | 2 | 01/31/2024 | Howmedica Osteonics Corp. |
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