Medical Device Recalls
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1 result found
510(K) Number: K042125 |
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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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Musculoskeletal Transplant Foundation, AFT Diverted Tube (3/4/Filled), indicated for treatment of su... | 2 | 06/16/2016 | Musculoskeletal Transplant Foundation, Inc. |
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