ClearanceBrief
510(k) K250866 ยท NKG Posterior Cervical Screw System

Sovereign Posterior Cervical System

ApplicantMet One Technologies, LLC, El Paso TX, US
DecisionSubstantially Equivalent, May 20, 2025
ReceivedMar 24, 2025
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K250866

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.