510(k) K181589 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Curiteva Lumbar Interbody Fusion System
| Applicant | Curiteva, LLC, Tanner AL, US |
| Decision | Substantially Equivalent, Dec 20, 2018 |
| Received | Jun 18, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181589
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.