510(k) K070631 ยท NKB Thoracolumbosacral Pedicle Screw System
DEVICE MODIFICATION TO RADIUS SPINAL SYSTEM
| Applicant | Stryker Spine, Allendale NJ, US |
| Decision | Substantially Equivalent, Jul 13, 2007 |
| Received | Mar 7, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K070631
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.