510(k) K092124 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
AXIALIF 2L, AXIALIF 2-LEVEL SYSTEM, AXIALIF APOLLO, AXIALIF II
| Applicant | Trans1 Incorporated, Wilmington NC, US |
| Decision | Substantially Equivalent, Jan 21, 2010 |
| Received | Jul 15, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092124
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.