ClearanceBrief
510(k) K083435 ยท KWS Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented

ARTHREX UNIVERS II SHOULDER PEGGED GLENOID

ApplicantArthrex, Inc., Naples FL, US
DecisionSubstantially Equivalent, Jun 26, 2009
ReceivedNov 20, 2008
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K083435

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.