510(k) K231781 ยท OQB Intervertebral Body Graft Containment Device
OptiMesh Multiplanar Expandable Interbody Fusion System
| Applicant | Spineology, Inc., Saint Paul MN, US |
| Decision | Substantially Equivalent, Oct 18, 2023 |
| Received | Jun 16, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K231781
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.