510(k) K213641 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
MONDRIAN ALIF Cage with Supplementary Fixation Plate
| Applicant | Ctl Medical Corporation, Addison TX, US |
| Decision | Substantially Equivalent, Sep 15, 2022 |
| Received | Nov 18, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K213641
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.