Medical Device Recalls
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1 result found
510(K) Number: K153122 |
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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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Endoskeleton" TCS Interbody System with Titan nanoLOCK" Surface Technology, NanoLock, 6 Deg, Interbo... | 2 | 10/12/2021 | Medtronic Sofamor Danek USA Inc |
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