510(k) K092536 ยท NKB Thoracolumbosacral Pedicle Screw System
SPINAL FIXATION SYSTEM
| Applicant | Lanx, Inc., Philadelphia PA, US |
| Decision | Substantially Equivalent, Oct 30, 2009 |
| Received | Aug 19, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092536
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.