510(k) K220902 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Navagio Lumbar Cage
| Applicant | Kalitec Medical, LLC, Orlando FL, US |
| Decision | Substantially Equivalent, May 27, 2022 |
| Received | Mar 28, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220902
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.