ClearanceBrief
510(k) K082236 ยท NKB Thoracolumbosacral Pedicle Screw System

CD HORIZON SPINAL SYSTEM

ApplicantMedtronic Sofamor Danek, Memphis TN, US
DecisionSubstantially Equivalent, Oct 10, 2008
ReceivedAug 7, 2008
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K082236

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.