ClearanceBrief
510(k) K250948 ยท HRS Plate, Fixation, Bone

TriMed Fusion Cup System

ApplicantTriMed, Inc., Santa Clarita CA, US
DecisionSubstantially Equivalent, Apr 8, 2025
ReceivedMar 21, 2025
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K250948

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.