Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K122455 |
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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 Ex-Fix System (Small, Medium, Distraction Osteogenesis (DO) and Large) ; (S) intended... | 2 | 08/24/2015 | Synthes (USA) Products LLC |
Synthes External Fixation Systems (Small, Medium, Large and DO), bone fixation appliance components. | 2 | 06/19/2014 | Synthes, Inc. |
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