510(k) K173883 ยท KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
External Fixation System
| Applicant | Life Spine, Inc., Huntley IL, US |
| Decision | Substantially Equivalent, Sep 7, 2018 |
| Received | Dec 21, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173883
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.