510(k) K103383 ยท NKB Thoracolumbosacral Pedicle Screw System
SPARTEK VARIABLE ANGLE PEDICLE SCREW POSTERIOR FUSION SYSTEM
| Applicant | Spartek Medical, Inc., Alameda CA, US |
| Decision | Substantially Equivalent, Feb 17, 2011 |
| Received | Nov 18, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K103383
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.