510(k) K192863 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
MONDRIAN Lumbar Interbody Fusion Cage System
| Applicant | Ctl Medical Corporation, Addison TX, US |
| Decision | Substantially Equivalent, Aug 26, 2020 |
| Received | Oct 7, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K192863
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.