ClearanceBrief
510(k) K150918 ยท NKG Posterior Cervical Screw System

PASS OCT Spinal System

ApplicantMedicrea International SA, Neyron, FR
DecisionSubstantially Equivalent, Oct 16, 2015
ReceivedApr 6, 2015
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K150918

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.