ClearanceBrief
510(k) K243826 ยท PHX Shoulder Prosthesis, Reverse Configuration

SMR Reverse HP Shoulder System

ApplicantLima Corporate S.P.A., Udine, IT
DecisionSubstantially Equivalent, Jul 3, 2025
ReceivedDec 12, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K243826

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.