Mako Surgical Corporation
8 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| Partial Knee Application (PKA) (K142530) | Mako Surgical Corporation | 2015-09-16 |
| RESTORIS POROUS PARTIAL KNEE SYSTEM (K150410) | Mako Surgical Corporation | 2015-03-20 |
| MAKOPLASTY TOTAL HIP ALLPICATION, RIO STANDARD SYSTEM (K141989) | Mako Surgical Corporation | 2014-11-13 |
| RESTORIS MULTICOMPARTMENTAL KNEE SYSTEM (K133039) | Mako Surgical Corporation | 2013-12-10 |
| MAKOPLASTY TOTAL HIP APPLICATION, RIO STANDARD SYSTEM (K121064) | Mako Surgical Corporation | 2012-06-06 |
| RESTORIS PARTIAL KNEE APPLICATION (PKA), RIO STANDARD SYSTEM (K112507) | Mako Surgical Corporation | 2012-03-01 |
| RESTORIS MULTICOMPARTMENTAL KNEE (MCK) SYSTEM (K090763) | Mako Surgical Corporation | 2009-06-17 |
| MAKO MODULAR KNEE COMPARTMENTAL IMPLANT SYSTEM (K082172) | Mako Surgical Corporation | 2008-11-28 |
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Every clearance here is in the API, with alerts when new ones post.