510(k) K212930 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
LumiVy Lumbar IBF System
| Applicant | Vy Spine, LLC, Tallahassee FL, US |
| Decision | Substantially Equivalent, Feb 16, 2022 |
| Received | Sep 14, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212930
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.