FDA 510(k) Applications Submitted by SYNTHES INC

FDA 510(k) Number	Submission Date	Device Name	Applicant
K113251	11/03/2011	SYNTHES MATRIXMANDIBLE PERFORMED RECONSTRUCTION PLATES	SYNTHES INC
K111323	05/11/2011	SYNTHES SYNPOR HD POROUS POLYETHYLENE THRER DIMENSIONAL IMPLANTS	SYNTHES INC
K121502	05/21/2012	SYNTHES CURVILINEAR DISTRACTION SYSTEM	SYNTHES INC
K121574	05/30/2012	SYNTHES MATRIXMADIBLE PLATE AND SCREW SYSTEM	SYNTHES INC
K122647	08/30/2012	SYNTHES PATIENT SPECIFIC PLATE	SYNTHES INC
K113567	12/02/2011	SYNTHES MATRIXMADIBLE PLATE AND SCREW SYSTEM	SYNTHES INC
K112689	09/15/2011	SYNTHES STERNAL FIXATION SYSTEM	SYNTHES INC
K131792	06/18/2013	SYNTHECEL DURA REPAIR, SYNTHECEL DURA ONLAY	SYNTHES INC