ClearanceBrief
510(k) K063417 ยท NKB Thoracolumbosacral Pedicle Screw System

MODIFICATION TO CD HORIZON SPINAL SYSTEM

ApplicantMedtronic Sofamor Danek, Memphis TN, US
DecisionSubstantially Equivalent, Jan 18, 2007
ReceivedNov 13, 2006
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K063417

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.