510(k) K131521 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
VELOX ANTERIOR CERVICAL PLATE SYSTEM
| Applicant | Spinecraft, LLC, Westmont IL, US |
| Decision | Substantially Equivalent, Dec 24, 2013 |
| Received | May 28, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131521
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.