ClearanceBrief
510(k) K191575 ยท NKB Thoracolumbosacral Pedicle Screw System

ARx Spinal System

ApplicantLife Spine, Inc., Huntley IL, US
DecisionSubstantially Equivalent, Aug 8, 2019
ReceivedJun 14, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K191575

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.