510(k) K162136 ยท NKG Posterior Cervical Screw System
CastleLoc-S Posterior Cervical Fixation System; LnK Posterior Cervical Fixation System
| Applicant | L&K BIOMED Co., Ltd., Giheung-Gu, Yongin-Si, KR |
| Decision | Substantially Equivalent, Nov 3, 2016 |
| Received | Aug 1, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162136
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.