510(k) K153439 ยท NKG Posterior Cervical Screw System
PathLoc-C Posterior Cervical Fixation System
| Applicant | L&K BIOMED Co., Ltd., Giheung-Gu, Yongin-Si, KR |
| Decision | Substantially Equivalent, Jul 21, 2016 |
| Received | Nov 27, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K153439
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.