510(k) K221776 ยท NKB Thoracolumbosacral Pedicle Screw System
NextGen Pedicle Screw System
| Applicant | Corelink, LLC, St. Louis MO, US |
| Decision | Substantially Equivalent, Aug 9, 2022 |
| Received | Jun 21, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221776
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.