ClearanceBrief
510(k) K000232 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

ROTAGLIDE + MODULAR KNEE SYSTEM WITH FIXED MENISCUS

ApplicantCorin USA, Tampa FL, US
DecisionSubstantially Equivalent, Feb 25, 2000
ReceivedJan 27, 2000
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K000232

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.