510(k) K220523 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
restor3d TiDAL Lumbar Interbody Fusion Device
| Applicant | Restor3D, Durham NC, US |
| Decision | Substantially Equivalent, Jun 17, 2022 |
| Received | Feb 23, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220523
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.