510(k) K202637 ยท MQP Spinal Vertebral Body Replacement Device
F3D Corpectomy System
| Applicant | Corelink, LLC, St. Louis MO, US |
| Decision | Substantially Equivalent, Dec 23, 2020 |
| Received | Sep 11, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202637
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.