Medical Device Recalls
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1 result found
510(K) Number: K860018 |
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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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Offset Wire Fixation Bolt, catalog number 8180-50-006. The bolts are used with the DePuy Ace-Fische... | 2 | 01/11/2012 | DePuy Orthopaedics, Inc. |
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