510(k) K143278 ยท KWP Appliance, Fixation, Spinal Interlaminal
LnK Posterior Cervical Fixation System
| Applicant | L&K BIOMED Co., Ltd., Giheung-Gu, Yongin-Si, KR |
| Decision | Substantially Equivalent, Jul 29, 2015 |
| Received | Nov 14, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K143278
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.