510(k) K200880 ยท HSB Rod, Fixation, Intramedullary And Accessories
T2 Tibial Nailing System, T2 Femoral Nail System, T2 Supracondylar Nail System, T2 Recon Nail System, T2 Greater Trochanter Nail (GTN),T2 Ankle Arthrodesis Nail,T2 Arthrodesis Nail System
| Applicant | Stryker GmbH, Mahwah NJ, US |
| Decision | Substantially Equivalent, Jul 1, 2020 |
| Received | Apr 2, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K200880
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.