510(k) K190016 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
Lateral Plate System
| Applicant | Corelink, LLC, St. Louis MO, US |
| Decision | Substantially Equivalent, Jun 12, 2019 |
| Received | Jan 3, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190016
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.