510(k) K122910 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
ARCHON ANTERIOR CERVICAL PLATE SYSTE,
| Applicant | Nu Vasive, Incorporated, San Diego CA, US |
| Decision | Substantially Equivalent, Oct 11, 2012 |
| Received | Sep 21, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K122910
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.