510(k) K210800 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
IO Expandable Lumbar Interbody Fusion System
| Applicant | MiRus, LLC, Marietta GA, US |
| Decision | Substantially Equivalent, Aug 20, 2021 |
| Received | Mar 16, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K210800
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.