510(k) K123809 ยท NKB Thoracolumbosacral Pedicle Screw System
CD HORIZON SPINAL SYSTEM
| Applicant | Medtronic Sofamor Danek USA, Inc., Memphis TN, US |
| Decision | Unknown, Feb 22, 2013 |
| Received | Dec 11, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K123809
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.