ClearanceBrief
510(k) K832302 ยท MBV Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uhmwpe, Pegged, Cemented, Polymer/Metal/Polymer

MARK I TOTAL KNEE SYS. ARTHROPLASTY

ApplicantAdvanced Biosearch Assn., Walker MI, US
DecisionSubstantially Equivalent, Aug 16, 1983
ReceivedJul 14, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K832302

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.