510(k) K160631 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Keos Lumbar IBFD
| Applicant | Keos, Lancaster PA, US |
| Decision | Substantially Equivalent, Jul 15, 2016 |
| Received | Mar 7, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160631
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.