510(k) K162250 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
FortiBridge Anterior Cervical Plate System
| Applicant | Nanovis Spine, LLC, Columbia City IN, US |
| Decision | Substantially Equivalent, Oct 26, 2016 |
| Received | Aug 10, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K162250
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.