ClearanceBrief
510(k) K153240 ยท OLO Orthopedic Stereotaxic Instrument

Styrker OrthoMap Express Knee System

ApplicantStryker Corporate, Freiburg, Baden-Wuerttemberg, DE
DecisionSubstantially Equivalent, Jul 7, 2016
ReceivedNov 9, 2015
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K153240

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.