510(k) K210539 ยท NKB Thoracolumbosacral Pedicle Screw System
CoreLink Midline Fixation System
| Applicant | Corelink, LLC, St. Louis MO, US |
| Decision | Substantially Equivalent, Apr 15, 2021 |
| Received | Feb 24, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K210539
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.