ClearanceBrief
510(k) K222291 ยท OLO Orthopedic Stereotaxic Instrument

Paradigm System

ApplicantProprio, Inc., Seattle WA, US
DecisionSubstantially Equivalent, Apr 21, 2023
ReceivedAug 1, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K222291

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.