510(k) K180373 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
CancelleX Porous Titanium Lumbar Interbody Device
| Applicant | Xenco Medical, LLC, San Diego CA, US |
| Decision | Substantially Equivalent, Aug 24, 2018 |
| Received | Feb 12, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180373
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.