510(k) K073643 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
TRANS1 AXIALIF 2-LEVEL OR II SYSTEM
| Applicant | Trans1 Incorporated, Wilmington NC, US |
| Decision | Substantially Equivalent, Apr 28, 2008 |
| Received | Dec 26, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073643
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.