ClearanceBrief
510(k) K071379 ยท PHX Shoulder Prosthesis, Reverse Configuration

DELTA XTEND REVERSE SHOULDER MODULAR STEM

ApplicantDePuy Orthopaedics, Inc., Warsaw IN, US
DecisionSubstantially Equivalent, Sep 11, 2007
ReceivedMay 17, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K071379

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.