Medical Device Recalls
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1 result found
510(K) Number: K241875 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| iNSitu Bipolar Hip System, Bipolar head implant Part ID Description 10-22-0038 Bipolar Head Asse... | 2 | 10/21/2025 | Theken Companies LLC |
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