The following data is part of a premarket notification filed by L&k Biomed Co., Ltd. with the FDA for Castleloc-p Anterior Cervical Plate System.
Device ID | K190425 |
510k Number | K190425 |
Device Name: | CastleLoc-P Anterior Cervical Plate System |
Classification | Appliance, Fixation, Spinal Intervertebral Body |
Applicant | L&K BIOMED Co., Ltd. #201, 202 16-25, Dongbaekjungang-ro 16 Beon-gil, Giheung-gu Yongin-si, KR 17015 |
Contact | Jihyeon Seo |
Correspondent | Jihyeon Seo L&K BIOMED Co., Ltd. #201, 202 16-25, Dongbaekjungang-ro 16 Beon-gil, Giheung-gu Yongin-si, KR 17015 |
Product Code | KWQ |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2019-02-22 |
Decision Date | 2019-03-21 |