510(k) K231840 ยท NKG Posterior Cervical Screw System
CastleLoc-S Posterior Cervical Fixation System
| Applicant | L&K BIOMED Co., Ltd., Yongin-Si, KR |
| Decision | Substantially Equivalent, Jul 20, 2023 |
| Received | Jun 22, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K231840
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.