FDA 510(k) Applications Submitted by SYNTHES SPINE CO.LP

FDA 510(k) Number	Submission Date	Device Name	Applicant
K052151	08/08/2005	SYNTHES PANGEA MONOAXIAL SYSTEM	SYNTHES SPINE CO.LP
K053508	12/16/2005	SYNFIX-LR	SYNTHES SPINE CO.LP
K061891	07/03/2006	SYNEX II	SYNTHES SPINE CO.LP
K062083	07/21/2006	SYNFIX -LR	SYNTHES SPINE CO.LP
K062933	09/28/2006	SYNTHES ORACLE SPACER	SYNTHES SPINE CO.LP
K103320	11/12/2010	SYNTHES XRL	SYNTHES SPINE CO.LP
K080020	01/03/2008	ARCOFIX	SYNTHES SPINE CO.LP
K081568	06/04/2008	ANTEGRA-T	SYNTHES SPINE CO.LP
K121852	06/25/2012	SYNTHES ZERO-P VARIABLE ANGLE (VA)	SYNTHES SPINE CO.LP
K112068	07/20/2011	SYNTHES ZERO-P VARIABLE ANGLE (VA)	SYNTHES SPINE CO.LP
K112459	08/26/2011	SYNTHES ZERO-P	SYNTHES SPINE CO.LP
K050451	02/22/2005	SYNTHES VECTRA SYSTEM	SYNTHES SPINE CO.LP
K070573	02/28/2007	SYNAPSE SYSTEM	SYNTHES SPINE CO.LP
K072253	08/14/2007	SYNFIX-LR SPACER	SYNTHES SPINE CO.LP
K072434	08/29/2007	SYNTHES OC FUSION AND SYNAPSE SYSTEMS	SYNTHES SPINE CO.LP
K063158	10/17/2006	SYNTHES ANTEGRA SYSTEM	SYNTHES SPINE CO.LP
K072981	10/23/2007	SYNTHES ZERO-P	SYNTHES SPINE CO.LP
K053418	12/08/2005	SYNTHES OC FUSION SYSTEM	SYNTHES SPINE CO.LP