510(k) K234087 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
restor3d TIDAL Lumbar Interbody Fusion System
| Applicant | Restor3D, Durham NC, US |
| Decision | Substantially Equivalent, Jan 22, 2024 |
| Received | Dec 22, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K234087
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.