Medical Device Recalls
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1 result found
510(K) Number: K043263 |
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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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Ulnar Osteotomy Compression Plate, Short Model: UOCP-S Product Usage: The UOCP-S is provided no... | 2 | 08/18/2018 | TriMed Inc. |
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