ClearanceBrief
510(k) K223927 ยท OLO Orthopedic Stereotaxic Instrument

360CAS

ApplicantKico Knee Innovation Company Pty Limited, Sydney, AU
DecisionSubstantially Equivalent, Jan 27, 2023
ReceivedDec 30, 2022
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K223927

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.