510(k) K162879 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Elite Expandable Interbody Fusion Device
| Applicant | Spineology, Inc., St. Paul MN, US |
| Decision | Substantially Equivalent, Jan 30, 2017 |
| Received | Oct 14, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162879
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.