Medical Device Recalls
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1 result found
510(K) Number: K092331 |
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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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LIMA Modular Revision Hip Stem Model 428-01-050_110 Product Usage: The Modular Revision Femoral ... | 2 | 02/11/2017 | Encore Medical, Lp |
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