ClearanceBrief
510(k) K233408 · QHE Shoulder Arthroplasty Implantation System

Materialise Shoulder System™, Materialise Shoulder Guide and Models, SurgiCase Shoulder Planner

ApplicantMaterialise NV, Leuven, BE
DecisionSubstantially Equivalent, Nov 9, 2023
ReceivedOct 6, 2023
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K233408

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.