FDA 510(k) Applications Submitted by CHRISTOPHER MCLEAN

FDA 510(k) Number	Submission Date	Device Name	Applicant
K110054	01/07/2011	NAVITRACK SYSTEM - OS KNEE UNIVERSAL, CAS SAME INCISION TIBIA REFERENCE	ZIMMER CAS
K060336	02/10/2006	NAVITRACK SYSTEM-OS KNEE UNIVERSAL, MODEL PRO-05002	ORTHOSOFT, INC.
K100599	03/03/2010	CAS FIXATION PIN 3.2 DIA X 180 MM STR, CAS FIXATON PIN 3.2 DIA X 80 MM STR, CAS FIXATON PIN 3.2 DIA X 150 MM	ORTHOSOFT, INC.
K030827	03/14/2003	NAVITRACK SYSTEM: TOTAL HIP REPLACEMENT CT-FREE CUP, MODEL 900.204	ORTHOSOFT, INC.
K150730	03/20/2015	Zimmer PSI Shoulder System	ZIMMER
K031156	04/11/2003	NAVITRACK SYSTEM-FLUOROSPINE, MODEL 900.005	ORTHOSOFT, INC.
K131409	05/15/2013	CAS PSI KNEE SYSTEM	ORTHOSOFT, INC.
K041369	05/24/2004	NAVITRACK SYSTEM - S&N IMAGE FREE HIP, MODEL PRO-03017	ORTHOSOFT, INC.
K021760	05/29/2002	NAVITRACK SYSTEM-OPTICAL TKR CT-LESS, MODEL 900.120	ORTHOSOFT, INC.
K141601	06/16/2014	IASSIST KNEE SYSTEM	ZIMMER CAS
K071714	06/22/2007	NAVITRACK SYSTEM - OS UNICONDYLAR KNEE UNIVERSAL, MODEL# PRO-06003	ORTHOSOFT, INC.
K071929	07/13/2007	NAVITRACK SYSTEM- PARTIAL HIP RESURFACING UNIVERSAL	ORTHOSOFT, INC.
K022364	07/22/2002	NAVITRACK SYSTEM TOTAL HIP REPLACEMENT,MODEL 900.200	ORTHOSOFT, INC.
K122326	08/01/2012	SMARTTOOLS KNEE SYSTEM	ZIMMER
K032917	09/22/2003	NAVITRACK SYSTEM - TOTAL HIP REPLACEMENT CT-FREE	ORTHOSOFT, INC.
K043536	12/22/2004	NAVITRACK SYSTEM - S&N IMAGE FREE KNEE	ORTHOSOFT, INC.