ClearanceBrief
510(k) K253941 · NKB Thoracolumbosacral Pedicle Screw System

CD Horizon™ ModuLeX™ Spinal System (LigaMAS Head Assembly)

ApplicantMedtronic Sofamor Danek USA, Inc., Memphis TN, US
DecisionSubstantially Equivalent, Jan 7, 2026
ReceivedDec 9, 2025
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K253941

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.