510(k) K241468 · MQP Spinal Vertebral Body Replacement Device
Vertiwedge® Intraosseous System
| Applicant | Foundation Surgical Group, Inc., Scottsdale AZ, US |
| Decision | Substantially Equivalent, Nov 7, 2024 |
| Received | May 24, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241468
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.