Medical Device Recalls
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1 result found
510(K) Number: K112463 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Ball Head, 28 Short CERAMIC Ball Head, 28 Medium CERAMIC Ball Head, 28 Long CERAMIC Ball Head, 32... | 2 | 05/24/2013 |
FEI # 3004022256 Orthopedic Alliance LLC |
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