510(k) K180025 ยท NKG Posterior Cervical Screw System
Centurion POCT System
| Applicant | Orthofix, Inc., Lewisville TX, US |
| Decision | Substantially Equivalent, Jan 22, 2018 |
| Received | Jan 3, 2018 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K180025
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.