510(k) K251302 ยท OQB Intervertebral Body Graft Containment Device
OptiMesh Multiplanar Expandable Interbody Fusion System
| Applicant | Spineology, Inc., Saint Paul MN, US |
| Decision | Substantially Equivalent, Dec 15, 2025 |
| Received | Apr 28, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K251302
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.