Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K130595 |
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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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TIBIO FEM/FEM NAIL. | 2 | 12/27/2013 | Zimmer, Inc. |
TIB NAIL | 2 | 12/27/2013 | Zimmer, Inc. |
NGK Stem Ext 24 x 245mm | 2 | 12/27/2013 | Zimmer, Inc. |
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