510(k) K131980 ยท NKB Thoracolumbosacral Pedicle Screw System
SEQUOIA PEDICLE SCREW SYSTEM INCLUDING SPEEDLINK II TRANSVERSE CONNECTOR SYSTEM
| Applicant | Zimmer Spine, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Sep 4, 2013 |
| Received | Jun 28, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131980
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.