ClearanceBrief
510(k) K220652 ยท OLO Orthopedic Stereotaxic Instrument

Knee 3

ApplicantBrainlab AG, Munich, DE
DecisionSubstantially Equivalent, Jun 3, 2022
ReceivedMar 7, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K220652

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.