ClearanceBrief
510(k) K883179 ยท KWL Prosthesis, Hip, Hemi-, Femoral, Metal

HIP FRACTURE STEM SYSTEM

ApplicantHowmedica Corp., Rutherford NJ, US
DecisionSubstantially Equivalent, Sep 22, 1988
ReceivedJul 27, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K883179

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.