510(k) K233509 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Zavation IBF System, Zavation Varisync Plate System and Varisync Spacer System, LABYRINTH System, Zavation ALIF System
| Applicant | Zavation Medical Products, LLC, Flowood MS, US |
| Decision | Substantially Equivalent, Apr 10, 2024 |
| Received | Oct 31, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233509
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.