Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K051948 |
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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 NRG Tibial Brg Insert Assy -Intended for knee replacement Part Number: 82-2-0910 ... | 2 | 01/31/2024 |
FEI # 3003070421 Howmedica Osteonics Corp. |
| SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3308 | 2 | 01/31/2024 |
FEI # 3003070421 Howmedica Osteonics Corp. |
| SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3110 | 2 | 01/31/2024 |
FEI # 3003070421 Howmedica Osteonics Corp. |
| SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3710 | 2 | 01/31/2024 |
FEI # 3003070421 Howmedica Osteonics Corp. |
| SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3708 | 2 | 01/31/2024 |
FEI # 3003070421 Howmedica Osteonics Corp. |
| SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3508 | 2 | 01/31/2024 |
FEI # 3003070421 Howmedica Osteonics Corp. |
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