FDA 510(k) Applications Submitted by SUSAN LEWANDOWSKI

FDA 510(k) Number	Submission Date	Device Name	Applicant
K050451	02/22/2005	SYNTHES VECTRA SYSTEM	SYNTHES SPINE CO.LP
K070573	02/28/2007	SYNAPSE SYSTEM	SYNTHES SPINE CO.LP
K150796	03/26/2015	Dental Bone Cutting Instruments	SYNTHES (USA) PRODUCTS, LLC
K141241	05/13/2014	MATRIXRIB ENDO THORACOSCOPIC RIB PLATING SYSTEM	SYNTHES (USA) PRODUCTS LLC
K051665	06/22/2005	SYNTHES VECTRA-T SYSTEM	SYNTHES SPINE
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
K092929	09/23/2009	SYNTHES MATRIX SYSTEM	SYNTHES (USA)
K063158	10/17/2006	SYNTHES ANTEGRA SYSTEM	SYNTHES SPINE CO.LP
K072981	10/23/2007	SYNTHES ZERO-P	SYNTHES SPINE CO.LP
K093464	11/06/2009	RAPIDSORB PLUS SCREW SYSTEM	SYNTHES (USA)
K143285	11/17/2014	Mandible External Fixator - MR Conditional	Synthes USA Products, LLC
K053418	12/08/2005	SYNTHES OC FUSION SYSTEM	SYNTHES SPINE CO.LP
K033844	12/11/2003	SYNTHES ANTERIOR CERVICAL COMPRESSION SYSTEM	SYNTHES (USA)
K153587	12/16/2015	Taps for Resorbable Screws	SYNTHES (USA) PRODUCTS LLC