Medical Device Recalls
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1 result found
510(K) Number: K992000 |
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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 Cranial Flap Tube Clamp and Crimping Device Product Usage: The Synthes Cranial Flap Tub... | 2 | 09/23/2015 | Synthes (USA) Products LLC |
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