510(k) K262712 · NKB Thoracolumbosacral Pedicle Screw System
Duet Spinal Fixation System
| Applicant | Duet Spine Holdings, LLC, Winona Lake IN, US |
| Decision | Substantially Equivalent, Sep 30, 2026 |
| Received | Jul 31, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K262712
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.