510(k) K182210 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
TiWAVE-L Porous Titanium Lumbar Cage
| Applicant | Kalitec Medical, LLC, Orlando FL, US |
| Decision | Substantially Equivalent, Jan 7, 2019 |
| Received | Aug 15, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182210
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.