Medical Device Recalls
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1 result found
510(K) Number: K223252 |
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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 Truliant, Activit-E Knee Insert, Catalog Numbers: a) 02-023-02-0029, b) 02-023-02-0032... | 2 | 01/18/2024 | Exactech, Inc. |
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