510(k) K233744 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Curiteva Porous PEEK Lumbar Interbody Fusion System
| Applicant | Curiteva, Inc., Tanner AL, US |
| Decision | Substantially Equivalent, Jan 18, 2024 |
| Received | Nov 22, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233744
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.