ClearanceBrief
510(k) K230366 ยท PHX Shoulder Prosthesis, Reverse Configuration

Arthrex Univers Revers Monoblock Stem Size 4/33

ApplicantArthrex, Inc., Naples FL, US
DecisionSubstantially Equivalent, Apr 10, 2023
ReceivedFeb 10, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K230366

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.