510(k) K140961 ยท KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
HOFFMANN LRF (LIMB RECONSTRUCTION FRAME) SYSTEM
| Applicant | Stryker Trauma AG, Selzach, CH |
| Decision | Substantially Equivalent, Nov 10, 2014 |
| Received | Apr 15, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K140961
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.