510(k) K102334 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
TRANS1 AXIALIF PLUS
| Applicant | Trans1 Incorporated, Wilmington NC, US |
| Decision | Substantially Equivalent, Mar 14, 2011 |
| Received | Aug 17, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102334
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.