510(k) K210155 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Duo Expandable Interbody Fusion System
| Applicant | Spineology, Inc., Saint Paul MN, US |
| Decision | Substantially Equivalent, Feb 19, 2021 |
| Received | Jan 21, 2021 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K210155
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.