Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K121220 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Exactech Equinoxe GLENOID,POSTERIOR AUGMENT, PEGGED, 16o, RIGHT, FOR CEMENTED USE ONLY, Mates with: ... | 2 | 03/29/2024 |
FEI # 1038671 Exactech, Inc. |
| Exactech Equinoxe GLENOID,POSTERIOR AUGMENT, PEGGED, 16o, LEFT, FOR CEMENTED USE ONLY, Mates with: ... | 2 | 03/29/2024 |
FEI # 1038671 Exactech, Inc. |
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