Medical Device Recalls
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1 result found
510(K) Number: K170593 |
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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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Makoplasty RIO Standard System; Ethernet to Fiber Optic Converter Catalog # 200933 Product Usage:... | 2 | 09/15/2018 | Mako Surgical Corporation |
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