510(k) K200922 ยท NKB Thoracolumbosacral Pedicle Screw System
Altus Spine HA Pedicle Screw System
| Applicant | Altus Partners, LLC, West Chester PA, US |
| Decision | Substantially Equivalent, Jan 26, 2021 |
| Received | Apr 6, 2020 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K200922
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.