510(k) K172941 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
CASCADIA Interbody System
| Applicant | K2m, Leesburg VA, US |
| Decision | Substantially Equivalent, Feb 12, 2018 |
| Received | Sep 26, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172941
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.