510(k) K222107 · NKG Posterior Cervical Screw System
Black Diamond POCT Spinal System
| Applicant | Osseus Fusion Systems, Dallas TX, US |
| Decision | Substantially Equivalent, Nov 3, 2022 |
| Received | Jul 18, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222107
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.