510(k) K062666 ยท MQP Spinal Vertebral Body Replacement Device
VUSION TS, PS, AND CS PARTIAL VERTEBRAL BODY REPLACEMENTS
| Applicant | Ortho Development Corp., Draper UT, US |
| Decision | Substantially Equivalent, Jan 25, 2007 |
| Received | Sep 7, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062666
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.