510(k) K192481 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
AccelFix Lumbar Plate System
| Applicant | L&K BIOMED Co., Ltd., Yongin-Si, KR |
| Decision | Substantially Equivalent, Jul 28, 2020 |
| Received | Sep 10, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K192481
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.