510(k) K161876 · JDQ Cerclage, Fixation
Tritium® Sternal Cable Plate System
| Applicant | Pioneer Surgical Technology, Inc., Dba Rti Surgical, Inc., Marquette MI, US |
| Decision | Substantially Equivalent, Sep 9, 2016 |
| Received | Jul 8, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K161876
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.