510(k) K890192 ยท KWP Appliance, Fixation, Spinal Interlaminal
LUQUE III SPINAL SYSTEM AND LUQUE MINI-SET
| Applicant | Danek Medical, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, Jan 4, 1990 |
| Received | Jan 18, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890192
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.