510(k) K241783 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
FortiVy OsteoVy Lumbar IBF
| Applicant | Vy Spine, LLC, Bountiful UT, US |
| Decision | Substantially Equivalent, Mar 18, 2025 |
| Received | Jun 20, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241783
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.