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Mako Surgical Corporation

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K133039	RESTORIS MULTICOMPARTMENTAL KNEE SYSTEM	NPJ	2013-12-10	View
510(k)	K121064	MAKOPLASTY TOTAL HIP APPLICATION, RIO STANDARD SYSTEM	OLO	2012-06-06	View
510(k)	K112507	RESTORIS PARTIAL KNEE APPLICATION (PKA), RIO STANDARD SYSTEM	OLO	2012-03-01	View
510(k)	K090763	RESTORIS MULTICOMPARTMENTAL KNEE (MCK) SYSTEM	NPJ	2009-06-17	View
510(k)	K082172	MAKO MODULAR KNEE COMPARTMENTAL IMPLANT SYSTEM	HSX	2008-11-28	View

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