FDA 510(k) Applications Submitted by Jonathan Reeves

FDA 510(k) Number	Submission Date	Device Name	Applicant
K150307	02/09/2015	RESTORIS Multicompartmental Knee System	MAKO SURGICAL CORP.
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
K142606	09/15/2014	Trident« Tritanium« PST« Acetabular Shells	MAKO Surgical Corp.
K133039	09/26/2013	RESTORIS MULTICOMPARTMENTAL KNEE SYSTEM	MAKO SURGICAL CORPORATION
K143635	12/22/2014	KINETIS Total Knee System	MAKO SURGICAL
K143752	12/31/2014	Total Knee Application (TKA)	MAKO SURGICAL CORP.