Medical Device Recalls
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1 result found
510(K) Number: K113364 |
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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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Drill Template and the Saw Guide for the Ulna Osteotomy System. Intended for fixation of fracture... | 2 | 03/25/2014 | Synthes, Inc. |
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