510(k) K182418 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
V3 Segmental Plating System
| Applicant | Atlas Spine, Inc., Jupiter FL, US |
| Decision | Substantially Equivalent, Nov 29, 2018 |
| Received | Sep 5, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182418
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.