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

FDA 510(k) Number Submission Date Device Name Applicant
K103414 11/22/2010 VENUS CERVICAL SPINAL FIXATION SYSTEM L&K BIOMED CO.,LTD.
K151677 06/22/2015 LnK Cervical Interbody Fusion Cage System L&K BIOMED Co.,Ltd.
K162136 08/01/2016 CastleLoc-S Posterior Cervical Fixation System; LnK Posterior Cervical Fixation System L&K BIOMED CO.,LTD.


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