510(k) K092325 ยท NKB Thoracolumbosacral Pedicle Screw System
MODIFICATION TO:CD HORIZON SPINAL SYSTEM
| Applicant | Medtronic Sofamor Danek USA, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, Dec 15, 2009 |
| Received | Aug 4, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K092325
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.