Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K170891 |
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Results per Page |
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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 |
FEI # 3005985723 Mako Surgical Corporation |
| Rio System Irrigation Clip - Catalog # 111690 Product Usage: The RESTORIS Partial Knee Applicati... | 2 | 08/14/2018 |
FEI # 3005985723 Mako Surgical Corporation |
| RESTORIS MCK TIBIAL BASEPLATE-RM/LL used in unicompartmental knee arthroplasty and knee replacements... | 2 | 05/04/2018 |
FEI # 3005985723 Mako Surgical Corporation |
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