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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
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