ClearanceBrief
510(k) K073676 ยท PHX Shoulder Prosthesis, Reverse Configuration

DEPUY DELTA XTEND REVERSE SHOULDER HIGH MOBILITY CUP

ApplicantDePuy Orthopaedics, Inc., Warsaw IN, US
DecisionSubstantially Equivalent, Jan 29, 2008
ReceivedDec 28, 2007
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K073676

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.