510(k) K172189 ยท HSB Rod, Fixation, Intramedullary And Accessories
Ins Hilden Humeral Arzzt, Ins Hilden Cannulated Tibial Arzzt, Ins Hilden Femoral Arzzt & Ins Hilden Retrograde Femoral Arzzt
| Applicant | Truemed Group, LLC, The Woodlands TX, US |
| Decision | Substantially Equivalent, Jan 16, 2018 |
| Received | Jul 20, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172189
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.