510(k) K183214 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
Raven Lumbar Plate System
| Applicant | Choicespine, LP, Knoxville TN, US |
| Decision | Substantially Equivalent, Jan 3, 2019 |
| Received | Nov 19, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K183214
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.