510(k) K133063 ยท NKB Thoracolumbosacral Pedicle Screw System
SANTIS PEDICLE SCREW SYSTEM
| Applicant | Lanterna Medical Technologies, Apple Valley MN, US |
| Decision | Substantially Equivalent, Jan 13, 2014 |
| Received | Sep 27, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133063
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.