Medical Device Recalls
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1 result found
510(K) Number: K010499 |
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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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Synthes Titanium Midface Distractor, MR Conditional, Part number 487.982. For temporary stabilizati... | 2 | 03/12/2013 | Synthes USA HQ, Inc. |
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