ClearanceBrief
510(k) K192080 ยท OLO Orthopedic Stereotaxic Instrument

iASSIST Knee System

ApplicantOrthosoft Inc (D/B/A Zimmer Cas), Montreal, CA
DecisionSubstantially Equivalent, Nov 5, 2019
ReceivedAug 2, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K192080

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.