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

FDA 510(k) Number Submission Date Device Name Applicant
K231839 06/22/2023 CastleLoc-P Anterior Cervical Plate System, AccelFix Lumbar Plate System L & K Biomed Co., Ltd.
K231840 06/22/2023 CastleLoc-S Posterior Cervical Fixation System L & K Biomed Co., Ltd.
K231841 06/22/2023 PathLoc SI Joint Fusion System L & K Biomed Co., Ltd.


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