510(k) K211323 ยท NKB Thoracolumbosacral Pedicle Screw System
ASTRA Spine System
| Applicant | Spinecraft, LLC, Westmont IL, US |
| Decision | Substantially Equivalent, Jun 3, 2021 |
| Received | Apr 30, 2021 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K211323
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.