ClearanceBrief
510(k) K223494 ยท NKB Thoracolumbosacral Pedicle Screw System

CD Horizon Spinal System

ApplicantMedtronic, Memphis TN, US
DecisionSubstantially Equivalent, Jan 23, 2023
ReceivedNov 21, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K223494

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.