510(k) K051678 ยท HSB Rod, Fixation, Intramedullary And Accessories
SYNTHES HINDFOOT ARTHRODESIS NAIL SYSTEM
| Applicant | Synthes (Usa), West Chester PA, US |
| Decision | Substantially Equivalent, Sep 21, 2005 |
| Received | Jun 23, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K051678
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Mar 1, 2024 | Synthes (USA) Products LLC 13 mm Titanium Hindfoot Arthrodesis Cannulated Nails EX, sterile -Intended to facilitate tibiotalocalcaneal arthrodesis to treat severe foot/ankle deformity, arthritis, instability, and skeletal defec Open, Classified |
HSB | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.