510(k) K163104 · KWQ Appliance, Fixation, Spinal Intervertebral Body
Terrace Anterior Cervical Plate System
| Applicant | Corelink, LLC, St. Louis MO, US |
| Decision | Substantially Equivalent, Jun 21, 2017 |
| Received | Nov 7, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K163104
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.