510(k) K994122 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
BONE GRAFT WASHER, MODEL 9090114 - 9090118
| Applicant | Danek Medical, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, Feb 18, 2000 |
| Received | Dec 7, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K994122
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.