510(k) K820034 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
ANTERIOR DISTRACTION SYSTEM
| Applicant | Stuart, Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 11, 1982 |
| Received | Jan 4, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820034
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.