510(k) K911307 ยท KWP Appliance, Fixation, Spinal Interlaminal
CROSSLINK PLATE
| Applicant | Danek Medical, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, Oct 24, 1991 |
| Received | Mar 25, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911307
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.