510(k) K172756 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Varian cage
| Applicant | Medyssey USA, Inc., Elk Grove Village IL, US |
| Decision | Substantially Equivalent, Dec 8, 2017 |
| Received | Sep 13, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172756
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.