Medical Device Recalls
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1 result found
510(K) Number: K070294 |
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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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| Synthes Titanium Trochanteric Fixation Nail (TFN)-Helical Blade Synthes Titanium Trochanteric Fix... | 2 | 11/20/2013 |
FEI # 3005180112 Synthes USA HQ, Inc. |
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