510(k) K240250 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
3D Printed PEEK Interbody System
| Applicant | Nvision Biomedical Technologies, Inc., San Antonio TX, US |
| Decision | Substantially Equivalent, Sep 17, 2024 |
| Received | Jan 30, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240250
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.