ClearanceBrief
510(k) K220452 ยท QHE Shoulder Arthroplasty Implantation System

Materialise Shoulder SystemTM Materialise Shoulder Guide and Models SurgiCase Shoulder Planner

ApplicantMaterialise NV, Leuven, BE
DecisionSubstantially Equivalent, Aug 17, 2022
ReceivedFeb 17, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K220452

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.