ClearanceBrief
510(k) K193633 · HRS Plate, Fixation, Bone

APTUS® Ankle Trauma System 2.8/3.5

ApplicantMedartis AG, Basel, CH
DecisionSubstantially Equivalent, Mar 26, 2020
ReceivedDec 27, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K193633

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.