ClearanceBrief
510(k) K210306 ยท NKB Thoracolumbosacral Pedicle Screw System

GII Spinal Fixation System

ApplicantColigne AG, Zurich, CH
DecisionSubstantially Equivalent, May 19, 2021
ReceivedFeb 3, 2021
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K210306

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.