ClearanceBrief
510(k) K113529 ยท NKB Thoracolumbosacral Pedicle Screw System

CD HORIZON VOYAGER SPINAL SYSTEM

ApplicantMedtronic Sofamor Danek, Memphis TN, US
DecisionUnknown, Feb 9, 2012
ReceivedNov 30, 2011
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K113529

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.