Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K103419 |
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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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Exactech Equinoxe GLENOID, POSTERIOR AUGMENT,PEGGED, CEMENTED, 8o, LEFT, Mates with: a) 38, 41, 4... | 2 | 03/29/2024 | Exactech, Inc. |
Exactech Equinoxe GLENOID, POSTERIOR AUGMENT,PEGGED, CEMENTED, 8o, RIGHT, Mates with: a) 38, 41, ... | 2 | 03/29/2024 | Exactech, Inc. |
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