ClearanceBrief
510(k) K972643 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

DEPUY AMK 3 PEG PATELLA

ApplicantDepuy, Inc., Warsaw IN, US
DecisionSubstantially Equivalent for Some Indications, Jan 21, 1998
ReceivedJul 15, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K972643

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.