510(k) K233234 ยท NKB Thoracolumbosacral Pedicle Screw System
PressON Spinal Fixation System
| Applicant | Nexus Spine, LLC, Salt Lake City UT, US |
| Decision | Substantially Equivalent, Oct 26, 2023 |
| Received | Sep 28, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K233234
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.