ClearanceBrief
510(k) K032033 ยท NKB Thoracolumbosacral Pedicle Screw System

CD HORIZON SPINAL SYSTEM

ApplicantMedtronic Sofamor Danek, Memphis TN, US
DecisionSubstantially Equivalent, Sep 12, 2003
ReceivedJul 1, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K032033

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.