Medical Device Recalls
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1 result found
510(K) Number: K093474 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| A.L.P.S. Foot Locking Calcaneus Plate,Small-Right. Provides the orthopaedic surgeon a means of bo... | 2 | 07/08/2015 |
FEI # 1825034 Biomet, Inc. |
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