ClearanceBrief
510(k) K132328 ยท NKB Thoracolumbosacral Pedicle Screw System

CD HORIZON SPINAL SYSTEM

ApplicantMedtronic Sofamor Danek USA, Inc., Memphis TN, US
DecisionSubstantially Equivalent, Dec 6, 2013
ReceivedJul 26, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K132328

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.