510(k) K163409 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Rampart(TM) T Lumbar Interbody Fusion Device
| Applicant | Spineology, Inc., Saint Paul MN, US |
| Decision | Substantially Equivalent, Mar 8, 2017 |
| Received | Dec 5, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K163409
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.