510(k) K173375 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
Anterior Cervical Plate System
| Applicant | Evolution Spine, LLC, Dallas TX, US |
| Decision | Substantially Equivalent, Dec 21, 2017 |
| Received | Oct 27, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173375
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.