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