510(k) K261809 · OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
Interwedge® Standalone Lateral
| Applicant | Foundation Surgical Group, Scottsdale AZ, US |
| Decision | Substantially Equivalent, Jul 31, 2026 |
| Received | Jun 1, 2026 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K261809
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.