510(k) K160522 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
White Pearl Preferred Angle Anterior Cervical Plate
| Applicant | Osseus Fusion Systems, LLC, Dallas TX, US |
| Decision | Substantially Equivalent, Apr 26, 2016 |
| Received | Feb 25, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160522
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.