ConforMIS Release: Arkansas Specialty Orthopedics to Host Clinical Trial of FDA Approved Personalized Knee Implant

LITTLEROCK, Ark.--(BUSINESS WIRE)--Researchers at Arkansas Specialty Orthopedics are participating in a ten year follow-up trial of the ConforMIS iUni® G2 knee resurfacing device, an FDA cleared implant for patients with osteoarthritic damage in a single compartment of the knee. Unlike traditional total knee replacement which replaces the entire joint, the ConforMIS partial knee resurfacing device allows for the targeted and minimally invasive treatment of just the diseased area of the knee in properly indicated patients.