510(k) K162264 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Cascadia Interbody System
| Applicant | K2m, Inc., Leesburg VA, US |
| Decision | Substantially Equivalent, Sep 21, 2016 |
| Received | Aug 11, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K162264
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.