Medical Device Recalls
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1 result found
510(K) Number: K141232 |
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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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APTUS Ulna Shortening 2.5 Product Usage: APTUS Ulna Shortening 2.5 Plates are indicated for fra... | 2 | 10/30/2014 | Medartis, Inc. |
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