ClearanceBrief
510(k) K192792 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body

TranS1 AxiaLIF Plus System

ApplicantTrans1, Wilmington NC, US
DecisionSubstantially Equivalent, Nov 20, 2019
ReceivedSep 30, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K192792

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.