Medical Device Recalls
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1 result found
510(K) Number: K132496 |
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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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| Total Toe Instrument Kit, Labeled in part: "Instrument Set, 15mm Toe, Dorsal Flange Combi" Part Numb... | 2 | 12/23/2015 |
FEI # 3004154314 Arthrosurface, Inc. |
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