ClearanceBrief
510(k) K192173 ยท OLO Orthopedic Stereotaxic Instrument

ROSA ONE Spine application

ApplicantMedtech S.A, Montpellier, FR
DecisionSubstantially Equivalent, Oct 29, 2019
ReceivedAug 12, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K192173

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.