ClearanceBrief
510(k) K231494 ยท OLO Orthopedic Stereotaxic Instrument

CoreLink Robotic Navigation Instruments

ApplicantCorelink, LLC, St. Louis MO, US
DecisionSubstantially Equivalent, Oct 27, 2023
ReceivedMay 23, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K231494

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.