Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K993956 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Fixed Open Screw (TI); 7.0MM (D) x 30MM (L); Made In USA, Biomet Spine, Parsippany, NJ 07054 Th... | 3 | 09/22/2009 | EBI, L.P. |
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