Medical Device Recalls
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1 result found
510(K) Number: K102990 |
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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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Femoral and Tibial Cutting Block Adapter Base. Brainlab knee, BrainLAB Image Guided Surgery System /... | 2 | 10/11/2018 | Brainlab AG |
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