ClearanceBrief
510(k) K181241 ยท DZJ Driver, Wire, And Bone Drill, Manual

KLS Martin Individual Patient Solutions (IPS) Planning System

ApplicantKLS-Martin L.P., Jacksonville FL, US
DecisionSubstantially Equivalent, Sep 13, 2018
ReceivedMay 10, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K181241

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.