510(k) K802222 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
ANTERIOR KYPHOSIS DISTRACTION DEVICE
| Applicant | Zimmer, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 10, 1980 |
| Received | Sep 12, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802222
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.