Medical Device Recalls
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1 result found
510(K) Number: K041085 |
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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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LPS Lower Extremity Dovetail Intercalary component. Intended for use in replacement of the mid-sh... | 1 | 07/31/2013 | DePuy Orthopaedics, Inc. |
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