510(k) K241487 · OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
Interwedge® Standalone Lateral
| Applicant | Foundation Surgical Group, Inc., Scottsdale AZ, US |
| Decision | Substantially Equivalent, Oct 2, 2024 |
| Received | May 24, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241487
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.