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 | K143271 |
510k Number | K143271 |
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 446-916 |
Contact | Ki-hyang Kim |
Correspondent | Yerim An L&K BIOMED Co., Ltd #201, 202 16-25, Dongbaekjungang-ro 16 Beon-gil Giheung-gu, Yongin-si, KR 446-916 |
Product Code | KWQ |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-11-13 |
Decision Date | 2015-07-01 |
Summary: | summary |