510(k) K970733 ยท HTY Pin, Fixation, Smooth
SYNTHES TITANIUM DIASTAL FEMORAL NAIL (TI DFN) SYSTEM
| Applicant | Synthes (Usa), Paoli PA, US |
| Decision | Substantially Equivalent, Apr 2, 1997 |
| Received | Feb 28, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970733
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Sep 18, 2013 | Synthes USA HQ, Inc. Synthes Cannulated Distal Femoral Nail (Trauma Nail), Part Number 450.851S, 420MM-Sterile. Orthppedic implant device. Terminated |
HTY | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.