Medical Device Recalls
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11 to 11 of 11 Results
Recall Date to: 02/26/2015 510(K) Number: K043547 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Biomet OSS Elliptical Proximal Femoral Trial 7 cm left provisional, stainless steel, Biomet Orthoped... | 2 | 06/29/2009 | Biomet, Inc. |
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