510(k) K150983 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
Pyrenees Cervical Plate System
| Applicant | K2m, Leesburg VA, US |
| Decision | Substantially Equivalent, Jul 14, 2015 |
| Received | Apr 14, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150983
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.