510(k) K181030 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Rubicon Lumbar Interbody Fusion System
| Applicant | Rubicon Spine, LLC, Sarasota FL, US |
| Decision | Substantially Equivalent, Jul 17, 2018 |
| Received | Apr 18, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181030
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.