Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K090763 |
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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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| Restoris MCK Onlay Insert Extractor. | 2 | 06/01/2018 |
FEI # 3005985723 Mako Surgical Corporation |
| Restoris Multicompartmental Knee (MCK) System RESTORIS MCK is indicated for single or multi-compa... | 2 | 03/01/2016 |
FEI # 3005985723 Mako Surgical Corporation |
| Restoris Multicompartmental Knee (MCK) System is an implant system designed to be used with MAKO's R... | 2 | 03/04/2014 |
FEI # 3005985723 Mako Surgical Corporation |
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