510(k) K132994 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
ANODYNE ANTERIOR CERVICAL PLATE SYSTEM
| Applicant | Corelink, LLC, Round Rock TX, US |
| Decision | Substantially Equivalent, Dec 5, 2013 |
| Received | Sep 24, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K132994
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.