510(k) K183682 ยท KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
OIC External Fixation System
| Applicant | Orthopaedic Implant Company, Reno NV, US |
| Decision | Substantially Equivalent, Apr 8, 2019 |
| Received | Dec 28, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K183682
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.