510(k) K094002 ยท NKB Thoracolumbosacral Pedicle Screw System
SPARTEK VARIABLE ANGLE PEDICLE SCREW POSTERIOR FUSION SYSTEM
| Applicant | Spartek Medical, Inc., Alameda CA, US |
| Decision | Substantially Equivalent, May 7, 2010 |
| Received | Dec 28, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K094002
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.