ClearanceBrief
510(k) K202771 ยท NKB Thoracolumbosacral Pedicle Screw System

CD Horizon Spinal System

ApplicantMedtronic, Memphis TN, US
DecisionSubstantially Equivalent, Oct 19, 2020
ReceivedSep 21, 2020
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K202771

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.