ClearanceBrief
510(k) K820755 ยท KWL Prosthesis, Hip, Hemi-, Femoral, Metal

THE ORIGINAL LEINBACH PLATFORM TOTAL HIP

ApplicantAllo Pro Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Jun 10, 1982
ReceivedMar 19, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K820755

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.