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FDA 510(k) Applications Submitted by HEE KYEONG JOO
FDA 510(k) Number
Submission Date
Device Name
Applicant
K120270
01/30/2012
VENUS SPINAL FIXATION SYSTEM
L&K BIOMED CO., LTD
K100706
03/12/2010
VENUS BASIC SPINAL FIXATION SYSTEM
L & K BIOMED CO., LTD
K110783
03/21/2011
VENUS INTERBODY FIXATION SYSTEM- VENUS PLIF/TLIF, ALIF PEEK CAGE
L & K BIOMED CO., LTD
K112643
09/12/2011
FOCUS MIS 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
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