Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K170891 |
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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 |
Rio System Irrigation Clip - Catalog # 111690 Product Usage: The RESTORIS Partial Knee Applicati... | 2 | 08/14/2018 | Mako Surgical Corporation |
RESTORIS MCK TIBIAL BASEPLATE-RM/LL used in unicompartmental knee arthroplasty and knee replacements... | 2 | 05/04/2018 | Mako Surgical Corporation |
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