FDA 510(k) Applications Submitted by MAKO SURGICAL CORPORATION

FDA 510(k) Number	Submission Date	Device Name	Applicant
K121064	04/06/2012	MAKOPLASTY TOTAL HIP APPLICATION, RIO STANDARD SYSTEM	MAKO SURGICAL CORPORATION
K112507	08/30/2011	RESTORIS PARTIAL KNEE APPLICATION (PKA), RIO STANDARD SYSTEM	MAKO SURGICAL CORPORATION
K150410	02/18/2015	RESTORIS POROUS PARTIAL KNEE SYSTEM	MAKO SURGICAL CORPORATION
K141989	07/22/2014	MAKOPLASTY TOTAL HIP ALLPICATION, RIO STANDARD SYSTEM	MAKO SURGICAL CORPORATION
K142530	09/09/2014	Partial Knee Application (PKA)	MAKO SURGICAL CORPORATION
K133039	09/26/2013	RESTORIS MULTICOMPARTMENTAL KNEE SYSTEM	MAKO SURGICAL CORPORATION
K090763	03/23/2009	RESTORIS MULTICOMPARTMENTAL KNEE (MCK) SYSTEM	MAKO SURGICAL CORPORATION
K082172	08/01/2008	MAKO MODULAR KNEE COMPARTMENTAL IMPLANT SYSTEM	MAKO SURGICAL CORPORATION