510(k) K131520 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
NEXUS ANTERIOR CERVICAL PLATE SYSTEM
| Applicant | Core-Nexus, Encino CA, US |
| Decision | Substantially Equivalent, Jul 11, 2013 |
| Received | May 28, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K131520
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.