510(k) K250072 · OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
CONDUIT SYNFIX Evolution Secured Spacer System
| Applicant | Avalign Technologies, Inc., Fort Wayne IN, US |
| Decision | Substantially Equivalent, Jul 10, 2025 |
| Received | Jan 10, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K250072
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.