FDA 510(k) Applications Submitted by SYNTHES USA

FDA 510(k) Number	Submission Date	Device Name	Applicant
K120070	01/09/2012	SYNTHES VARIABLE ANGLE LCP ELBOW SYSTEM	SYNTHES USA
K120717	03/08/2012	SYNTHES VARIABLE ANGLE LCP ELBOW SYSTEM (MEDICAL AND POSTEROLATERAL DISTAL HUMERUS PLATES)	SYNTHES USA
K120854	03/21/2012	SYNTHES VA LCP ANKLE TRAUMA SYSTEM	SYNTHES USA
K121601	06/01/2012	SYNTHES 2.7/3.5MM VARIABLE ANGLE LCP ANKLE TRAUMA SYSTEM-ANTEROLATERAL DISTAL TIBIA PLATE	SYNTHES USA
K141527	06/09/2014	DEPUY SYNTHES VARIABLE ANGLE LOCKING HAND SYSTEM	SYNTHES USA
K110592	03/02/2011	3.7MM/5.0MM DYNAMIC LOCKING SCREW	SYNTHES USA
K110125	01/18/2011	2.4 MM VA-LCP VOLAR RIM DISTAL RADIUS SYSTEM	SYNTHES USA
K120083	01/11/2012	SET SCREW FOR TI TROCHANTERIC FIXATION NAIL(TFN)	SYNTHES USA
K110354	02/07/2011	4.5MM VA-LCP CURVED CONDYLAR PLATE SYSTEM	SYNTHES USA