ClearanceBrief
510(k) K211958 ยท NKB Thoracolumbosacral Pedicle Screw System

CD Horizon Spinal System

ApplicantMedtronic Sofamor Danek USA, Inc., Memphis TN, US
DecisionSubstantially Equivalent, Jul 21, 2021
ReceivedJun 24, 2021
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K211958

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.