Medical Device Recalls
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1 to 8 of 8 Results
510(K) Number: K994128 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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SCORPIO TS TIB INSERT -Intended for knee replacement Part Number: 72-4-0321 | 2 | 01/31/2024 | Howmedica Osteonics Corp. |
SCORPIO TS TIB INSERT -Intended for knee replacement Part Number: 72-4-0510 | 2 | 01/31/2024 | Howmedica Osteonics Corp. |
SCORPIO TS TIB INSERT-Intended for knee replacement Part Number:72-4-7512 | 2 | 01/31/2024 | Howmedica Osteonics Corp. |
SCORPIO TS TIB INSERT -Intended for knee replacement Part Number: 72-4-7524 | 2 | 01/31/2024 | Howmedica Osteonics Corp. |
SCORPIO TS TIB INSERT -Intended for knee replacment Part Number: 72-4-7516 | 2 | 01/31/2024 | Howmedica Osteonics Corp. |
SCORPIO TS TIB INSERT. Intended for knee replacement Part Number: 72-4-7518 | 2 | 01/31/2024 | Howmedica Osteonics Corp. |
SCORPIO TS TIB INSERT -Intended for knee replacement Part Number: 72-4-7521 | 2 | 01/31/2024 | Howmedica Osteonics Corp. |
SCORPIO TS TIB INSERT -Intended for knee replacement Part Number: 72-4-7514 | 2 | 01/31/2024 | Howmedica Osteonics Corp. |
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