510(k) K250332 · NKG Posterior Cervical Screw System
Virage® OCT Spinal Fixation System
| Applicant | Highridge Medical, LLC, Westminister CO, US |
| Decision | Substantially Equivalent, Apr 4, 2025 |
| Received | Feb 5, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K250332
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.