510(k) K233947 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
KLIMT Expandable Lumbar Interbody Fusion (LIF) Cage System
| Applicant | Ctl Medical Corporation, Addison TX, US |
| Decision | Substantially Equivalent, Oct 10, 2024 |
| Received | Dec 14, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233947
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.