FDA 510(k) Applications Submitted by L&K BIOMED Co., Ltd

FDA 510(k) Number	Submission Date	Device Name	Applicant
K120270	01/30/2012	VENUS SPINAL FIXATION SYSTEM	L&K BIOMED CO., LTD
K120063	01/09/2012	VENUS LUMBAR INTERVERTEBRAL BODY FUSION CAGE SYSTEM	L&K BIOMED CO., LTD
K120140	01/18/2012	FOCUS SPINAL SYSTEM	L&K BIOMED CO., LTD
K103085	10/19/2010	VENUS BASIC SPINAL FIXATION SYSTEM	L&K BIOMED CO., LTD
K113509	11/28/2011	LEXUS ANTERIOR CERVICAL PLATE SYSTEM	L&K BIOMED CO., LTD
K120840	03/20/2012	LEXUS CERVICAL INTERVERTEBRAL BODY FUSION CAGE SYSTEM	L&K BIOMED CO., LTD
K143271	11/13/2014	CastleLoc-P Anterior Cervical Plate System	L&K BIOMED Co., Ltd
K151140	04/29/2015	LnK Lumbar Interbody Fusion Cage System	L&K BIOMED Co., Ltd
K143360	11/24/2014	LnK Cervical Interbody Fusion Cage System	L&K BIOMED Co., Ltd