510(k) K203308 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Ali Interbody Fusion System
| Applicant | Raed M. Ali, M.D., Inc., Newport Coast CA, US |
| Decision | Substantially Equivalent, Jan 15, 2021 |
| Received | Nov 10, 2020 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K203308
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.