510(k) K160906 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Rampart O Lumbar Interbody Fusion Device, Rampart T Lumbar Interbody Fusion Device, Rampart A lumbar Interbody Fusion Device
| Applicant | Spineology, Inc., St. Paul MN, US |
| Decision | Substantially Equivalent, Jul 14, 2016 |
| Received | Apr 1, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160906
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.