ClearanceBrief
510(k) K252352 ยท PHX Shoulder Prosthesis, Reverse Configuration

SMR Shoulder System; PRIMA Glenoid System; PRIMA Humeral System

ApplicantLima Corporate S.P.A., Villanova Di San Daniele, IT
DecisionSubstantially Equivalent, Jan 22, 2026
ReceivedJul 29, 2025
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K252352

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.