510(k) K252432 · ODP Intervertebral Fusion Device With Bone Graft, Cervical
Flex-Z Cervical Cage
| Applicant | Spinepoint, LLC, Reno NV, US |
| Decision | Substantially Equivalent, Mar 25, 2026 |
| Received | Aug 1, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K252432
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.