510(k) K211845 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Deploy Expandable Interbody System
| Applicant | Southern Spine, LLC, Macon GA, US |
| Decision | Substantially Equivalent, Nov 16, 2021 |
| Received | Jun 15, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211845
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.