ClearanceBrief
510(k) K222684 · NKB Thoracolumbosacral Pedicle Screw System

XIA® 4.5 Spinal System, XIA® 4.5 Cortical Trajectory, XIA® 3 Spinal System, Serrato® Spinal System, XIA® Growth Rod Conversion Set, XIA® II Spinal System, XIA® Precision System, XIA® Anterior, Diapason® Spinal System, Opus™ Spinal System, Radius® Spinal System, Mantis® Spinal System, Mantis® Redux,

ApplicantStryker Spine, Allendale NJ, US
DecisionSubstantially Equivalent, Jun 8, 2023
ReceivedSep 6, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K222684

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.