510(k) K151020 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Rampart-T Interbody Fusion System
| Applicant | Spineology, Inc., St. Paul MN, US |
| Decision | Substantially Equivalent, Jul 22, 2015 |
| Received | Apr 16, 2015 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K151020
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.