510(k) K203819 ยท HSB Rod, Fixation, Intramedullary And Accessories
T2 Alpha Femur Retrograde Nailing System, T2 Alpha Femur Antegrade GT/PF Nailing System, T2 Tibial Nailing System, T2 Femoral System, T2 Supracondylar Nail System
| Applicant | Stryker GmbH, Mahwah NJ, US |
| Decision | Substantially Equivalent, Feb 26, 2021 |
| Received | Dec 29, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K203819
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.