510(k) K160959 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Xsert Lumbar Expandable Interbody System
| Applicant | X-Spine Systems, Inc., Miamisburg OH, US |
| Decision | Substantially Equivalent, Nov 17, 2016 |
| Received | Apr 5, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160959
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.