Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K063279 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Novation Press-Fit Splined RDD, Extended Offset, HA Coated, 12/14 Taper Femoral Stems, Size 18. Fem... | 2 | 07/05/2016 |
FEI # 1038671 Exactech, Inc. |
| Novation Press-Fit Splined RDD, Extended Offset, HA Coated, 12/14 Taper Femoral Stems, Size 17. Pro... | 2 | 07/05/2016 |
FEI # 1038671 Exactech, Inc. |
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