FDA 510(k) Applications Submitted by DEBORAH JACKSON

FDA 510(k) Number	Submission Date	Device Name	Applicant
K061753	06/21/2006	SYNTHES (USA) CLAVICLE HOOK PLATES	SYNTHES (USA)
K060092	01/12/2006	QUICKCAT EXTRACTION CATHETER	KENSEY NASH CORP.
K071264	05/04/2007	SYNTHES (USA) 2.4/2.7 MM LOCKING FOOT MODULE	SYNTHES (USA)
K091618	06/03/2009	VITOMATRIX	ORTHOVITA, INC.
K061621	06/12/2006	SYNTHES (USA) 6.5 MM CANCELLOUS SCREWS	SYNTHES (USA)
K061973	07/12/2006	SYNTHES 3.5MM SPRING PLATE	SYNTHES (USA)
K102545	09/03/2010	FM-02 BONE GRAFT SUBSTITUTE	ORTHOVITA, INC.
K062872	09/26/2006	SYNTHES (USA) PEDIATRIC LCP HIP PLATE SYSTEM	SYNTHES (USA)
K063049	10/04/2006	SYNTHES (USA) MODULAR MINI FRAGMENT LCP SYSTEM	SYNTHES (USA)
K083033	10/10/2008	VITOSS BONE GRAFT SUBSTITUTE, BONE GRAFT SUBSTITUTE FILLED CANISTER, FOAM & BIOACTIVE FOAM BONE GRAFT SUBSTITUTE	ORTHOVITA, INC.
K063181	10/19/2006	SYNTHES (USA) CONDYLAR HEAD ADD-ON SYSTEM	SYNTHES (USA)
K103173	10/28/2010	VITOSS BA BIMODAL BIOACTIVE BONE GRAFT SUBSTITUTE	ORTHOVITA, INC.
K063473	11/16/2006	SYNTHES ORTHODONTIC BONE ANCHOR SYSTEM	SYNTHES (USA)
K063790	12/22/2006	THE SYNTHES MATRIXMANDIBLE PLATE AND SCREW SYSTEM	SYNTHES (USA)