Medical Device Recalls
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510(K) Number: K863668 |
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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| SCORPIO RECESSED PATELLA- Intended for Knee Replacement Part Number: 3044-0026 | 2 | 01/31/2024 |
FEI # 3003070421 Howmedica Osteonics Corp. |
| SCORPIO RECESSED PATELLA-Intended for knee repalcment Part Number: 3044-0032 | 2 | 01/31/2024 |
FEI # 3003070421 Howmedica Osteonics Corp. |
| SCORPIO RECESSED PATELLA- Intended for knee replacement Part Number: 3044-0030 | 2 | 01/31/2024 |
FEI # 3003070421 Howmedica Osteonics Corp. |
| SCORPIO RECESSED PATELLA- Intended for knee replacement Part Number: 3044-0028 | 2 | 01/31/2024 |
FEI # 3003070421 Howmedica Osteonics Corp. |
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