Medical Device Recalls
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1 result found
510(K) Number: K033618 |
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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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Synthes Trauma Nail System. The devices are indication for bone fixation. | 2 | 08/26/2013 | Synthes USA HQ, Inc. |
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