510(k) K173867 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
Axis Anterior Cervical Plate System
| Applicant | Axis Orthopaedics, Soldotna AK, US |
| Decision | Substantially Equivalent, Apr 5, 2018 |
| Received | Dec 20, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173867
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.