Medical Device Recalls
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1 result found
510(K) Number: K141993 |
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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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| Nakoma-SL Anterior Cervical Plating System's Variable Single Barrel Drill Guide Product Usage: T... | 2 | 07/07/2015 |
FEI # 3008520015 Alliance Partners LLC |
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