510(k) K123568 ยท KWP Appliance, Fixation, Spinal Interlaminal
VERTEX RECONSTRUCTION SYSTEM
| Applicant | Medtronic Sofamor Danek USA, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, Dec 18, 2012 |
| Received | Nov 20, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K123568
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.