510(k) K231359 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
RODIN Expandable Lumbar Cage System
| Applicant | Ctl Medical Corporation, Addison TX, US |
| Decision | Substantially Equivalent, Jun 9, 2023 |
| Received | May 10, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K231359
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.