ClearanceBrief
510(k) K192653 ยท OLO Orthopedic Stereotaxic Instrument

Perseus

ApplicantOrthokey Italia S.R.L., Carrara, IT
DecisionSubstantially Equivalent, Sep 9, 2020
ReceivedSep 24, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K192653

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.