ClearanceBrief
510(k) K192675 ยท HRS Plate, Fixation, Bone

VariAx Foot

ApplicantStryker GmbH, Mahwah NJ, US
DecisionSubstantially Equivalent, Nov 22, 2019
ReceivedSep 26, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K192675

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.