Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K060138 |
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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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DePuy Synthes Craniomaxillofacial Distraction System (AB Distractor Bodies and BC Distractor Bodies) | 1 | 08/20/2014 | Synthes, Inc. |
Synthes CMF Distraction System The product is intended for use as a bone stabilizer and lengtheni... | 2 | 07/12/2013 | Synthes USA HQ, Inc. |
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