ClearanceBrief
510(k) K063670 ยท NKB Thoracolumbosacral Pedicle Screw System

MODIFICATIONS TO CD HORIZON SPINAL SYSTEM

ApplicantMedtronic Sofamor Danek, Memphis TN, US
DecisionSubstantially Equivalent, Jun 28, 2007
ReceivedDec 11, 2006
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K063670

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.