510(k) K233807 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
LumiVy Lumbar IBF System
| Applicant | Vy Spine, LLC, Bountiful UT, US |
| Decision | Substantially Equivalent, Sep 24, 2024 |
| Received | Nov 29, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233807
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.