510(k) K180777 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
K2M Expandable Interbody System
| Applicant | K2m, Inc., Leesburg VA, US |
| Decision | Substantially Equivalent, Aug 3, 2018 |
| Received | Mar 26, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180777
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.