510(k) K223412 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
LumiVy Lumbar IBF System
| Applicant | Vy Spine, LLC, Tallahassee FL, US |
| Decision | Substantially Equivalent, Jan 6, 2023 |
| Received | Nov 9, 2022 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K223412
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.