ClearanceBrief
510(k) K220341 ยท NKB Thoracolumbosacral Pedicle Screw System

ARx Modular Spinal System

ApplicantLife Spine, Inc., Huntley IL, US
DecisionSubstantially Equivalent, May 2, 2022
ReceivedFeb 7, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K220341

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.