510(k) K181963 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ostaPek Interbody Fusion Cages
| Applicant | Coligne AG, Zurich, CH |
| Decision | Substantially Equivalent, Nov 14, 2018 |
| Received | Jul 23, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181963
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.