ClearanceBrief
510(k) K181824 ยท NKB Thoracolumbosacral Pedicle Screw System

CBT Screw Fixation System

ApplicantU&I Corporation, Uijeongbu-Si, KR
DecisionSubstantially Equivalent, Dec 13, 2018
ReceivedJul 9, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K181824

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.