ClearanceBrief
510(k) K042167 ยท NKB Thoracolumbosacral Pedicle Screw System

MODIFICATION TO: CD HORIZON SPINAL SYSTEM

ApplicantMedtronic Sofamor Danek, Memphis TN, US
DecisionSubstantially Equivalent, Sep 8, 2004
ReceivedAug 11, 2004
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K042167

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.