510(k) K171724 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Rampart L Lumbar Interbody Fusion Device
| Applicant | Spineology, Inc., Saint Paul MN, US |
| Decision | Substantially Equivalent, Jul 24, 2017 |
| Received | Jun 12, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K171724
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.