510(k) K050965 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
TRANS1 AXIALIF SYSTEM
| Applicant | Trans1 Incorporated, Wilmington NC, US |
| Decision | Substantially Equivalent, Jun 14, 2005 |
| Received | Apr 18, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K050965
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.