510(k) K233989 · NKG Posterior Cervical Screw System
CarboClear® Posterior Cervical Screw System
| Applicant | CarboFix Orthopedics , Ltd., Herzeliya, IL |
| Decision | Substantially Equivalent, Mar 27, 2024 |
| Received | Dec 18, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233989
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.