ClearanceBrief
510(k) K153589 ยท NKB Thoracolumbosacral Pedicle Screw System

CD HORIZON Spinal System

ApplicantMedtronic Sofamor Danek USA, Inc., Memphis TN, US
DecisionSubstantially Equivalent, Feb 10, 2016
ReceivedDec 16, 2015
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K153589

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.