510(k) K020384 ยท HSB Rod, Fixation, Intramedullary And Accessories
T2 ARTHRODESIS NAIL SYSTEM
| Applicant | Howmedica Osteonics Corp., Allendale NJ, US |
| Decision | Substantially Equivalent, May 6, 2002 |
| Received | Feb 5, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020384
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 16, 2012 | Stryker Howmedica Osteonics Corp. Stryker T2 Arthrodesis Nailing System. Manufacturer: Stryker Trauma GmbH, Professor-Kuntscher-Str. 1-5, 24232 Schonkirchen Germany. Distributed in the USA by Stryker Orthopaedics, 325 Corporate Driv Terminated |
HSB | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.