Medical Device Recalls
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1 result found
510(K) Number: K120507 |
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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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Femoral component, CR, cemented, #1, left 2103-1310 Femoral component, CR, cemented, #2, left 2103-... | 2 | 05/24/2013 | Orthopedic Alliance LLC |
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