510(k) K160125 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Cascadia Interbody System
| Applicant | K2m, Leesburg VA, US |
| Decision | Substantially Equivalent, Apr 22, 2016 |
| Received | Jan 20, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160125
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.