ClearanceBrief
510(k) K122442 ยท PHX Shoulder Prosthesis, Reverse Configuration

DEPUY CTA REVERSE SHOULDER SYSTEM

ApplicantDepuy France, Warsaw IN, US
DecisionSubstantially Equivalent, Sep 6, 2012
ReceivedAug 10, 2012
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K122442

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.