ClearanceBrief
510(k) K090103 ยท MAY Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous Cemented, Osteophilic Finish

100KGY E-POLY ACETABULAR LINERS- ADDITIONAL PROFILES: +3 MAXROM AND +3 HI-WALL

ApplicantBiomet, Inc., Warsaw IN, US
DecisionSubstantially Equivalent, Feb 11, 2009
ReceivedJan 15, 2009
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K090103

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.