ClearanceBrief
510(k) K962646 ยท KWL Prosthesis, Hip, Hemi-, Femoral, Metal

PRIME MODULAR ENDO HEAD

ApplicantOrthopaedic Innovations, Inc., Minneapolis MN, US
DecisionSubstantially Equivalent, Sep 23, 1996
ReceivedJul 8, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K962646

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.