510(k) K103137 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
VENUS ANTERIOR CERVICAL PLATE
| Applicant | Verticor, Ltd., Round Rock TX, US |
| Decision | Substantially Equivalent, Feb 10, 2011 |
| Received | Oct 25, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K103137
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.