ClearanceBrief
510(k) K130646 ยท NKB Thoracolumbosacral Pedicle Screw System

CD HORIZON SPINAL SYSTEM

ApplicantMedtronic Sofamor Danek USA, Inc., Memphis TN, US
DecisionUnknown, Apr 10, 2013
ReceivedMar 11, 2013
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K130646

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.