510(k) K223627 · KWQ Appliance, Fixation, Spinal Intervertebral Body
PreView-III Anterior Cervical Plate System
| Applicant | Nexus Spine, LLC, Salt Lake City UT, US |
| Decision | Substantially Equivalent, Feb 2, 2023 |
| Received | Dec 5, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223627
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.