510(k) K091365 ยท KWP Appliance, Fixation, Spinal Interlaminal
VERTEX RECONSTRUCTION SYSTEM, VERTEX SELECT RECONSTRUCTION SYSTEM
| Applicant | Medtronic Soafamor Danek, Memphis TN, US |
| Decision | Substantially Equivalent, Aug 6, 2009 |
| Received | May 8, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091365
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.