ClearanceBrief
510(k) K060707 ยท KWY Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented

AESCULAP BIPOLAR ACETABULAR CUP

ApplicantAesculap, Inc., Center Valley PA, US
DecisionSubstantially Equivalent, May 31, 2006
ReceivedMar 16, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K060707

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.