510(k) K200596 · PML Bone Cement, Posterior Screw Augmentation
G21 Cement, VADER® Pedicle System
| Applicant | Icotec AG, 9450 Altstaetten (Sg), CH |
| Decision | Substantially Equivalent, Oct 13, 2020 |
| Received | Mar 6, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K200596
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Dec 19, 2022 | Icotec Ag VADER Pedicle System Torque Wrench, Hudson Coupling, 12 Nm, REF 42-702 Terminated |
NKB | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.