NCT03289000View on ClinicalTrials.gov

A Retrospective Study to Evaluate the ConforMIS iTotal® Posterior Stabilized (PS) Knee Replacement System

CompletedOBSERVATIONAL
Enrollment

93

Participants

Timeline

Start Date

April 24, 2017

Primary Completion Date

August 4, 2017

Study Completion Date

December 31, 2017

Conditions
Osteo Arthritis Knee
Interventions
DEVICE

iTotal Posterior Stabilized (PS) Knee Replacement System

Patient-specific posterior stabilized total knee replacement and patient specific surgical jigs

Trial Locations (2)

25702

Scott Orthopedic Center, Huntington

37203

Tennessee Orthopaedic Alliance, Nashville

Sponsors

Lead Sponsor

Restor3D
All Listed Sponsors
lead

Restor3D

INDUSTRY