ClearanceBrief
510(k) K233725 ยท OLO Orthopedic Stereotaxic Instrument

Spine Navigation System

ApplicantMedivis, Inc., New York NY, US
DecisionSubstantially Equivalent, Jul 26, 2024
ReceivedNov 21, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K233725

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.