510(k) K080020 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
ARCOFIX
| Applicant | Synthes Spine Co.Lp, West Chester PA, US |
| Decision | Substantially Equivalent, May 23, 2008 |
| Received | Jan 3, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080020
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.