ClearanceBrief
510(k) K234047 ยท OLO Orthopedic Stereotaxic Instrument

Automatic Registration

ApplicantBrainlab AG, Munich, DE
DecisionSubstantially Equivalent, Mar 20, 2024
ReceivedDec 21, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K234047

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.