ClearanceBrief
510(k) K090390 ยท NKB Thoracolumbosacral Pedicle Screw System

CD HORIZON SPINAL SYSTEM

ApplicantMedtronic Sofamor Danek, Memphis TN, US
DecisionSubstantially Equivalent, May 15, 2009
ReceivedFeb 17, 2009
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K090390

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.