ClearanceBrief
510(k) K900051 ยท KWY Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented

MOORE TYPE ENDO PROSTHESIS

ApplicantLima Intl. Corp., E Providence RI, US
DecisionSubstantially Equivalent, Oct 3, 1990
ReceivedJan 3, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K900051

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.