510(k) K182473 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
PYRENEES Cervical Plate System, BLUE RIDGE Cervical Plate System, OZARK Cervical Plate System, CAYMAN Thoracolumbar and Buttress Plate Systems
| Applicant | K2m, Inc., Leesburg VA, US |
| Decision | Substantially Equivalent, Dec 12, 2018 |
| Received | Sep 10, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182473
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.