Medical Device Recalls
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1 result found
510(K) Number: K202858 |
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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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Flex-Thread Inserter Shaft intended for Fibula intramedullary-intended to be used with the Inserter... | 2 | 01/03/2022 | Flower Orthopedics Corporation |
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