ClearanceBrief
510(k) K000254 ยท JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented

PAR 5 ACETABULAR COMPONENT

ApplicantBiomet, Inc., Warsaw IN, US
DecisionSubstantially Equivalent, Feb 7, 2000
ReceivedJan 28, 2000
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K000254

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.