510(k) K052402 ยท KWP Appliance, Fixation, Spinal Interlaminal
VERTEX RECONSTRUCTION SYSTEM
| Applicant | Medtronic Sofamor Danek, Memphis TN, US |
| Decision | Substantially Equivalent, Sep 23, 2005 |
| Received | Sep 1, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K052402
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.