510(k) K052404 ยท KWP Appliance, Fixation, Spinal Interlaminal
DENALI DEFORMITY SYSTEM
| Applicant | K2m, LLC, Leesburg VA, US |
| Decision | Substantially Equivalent, May 23, 2006 |
| Received | Sep 1, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K052404
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.