A Retrospective Study to Evaluate the ConforMIS iTotal® Posterior Stabilized (PS) Knee Replacement System
NCT03289000 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 93
Last updated 2023-10-25
Summary
This study is a retrospective, multi-center study, with one single remote follow up contact. This study will include a minimum of 80 patients and a maximum 100 patients who have been treated with the ConforMIS iTotal PS knee product.
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
Sponsors & Collaborators
-
Restor3D
lead INDUSTRY
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2017-04-24
- Primary Completion
- 2017-08-04
- Completion
- 2017-12-31
- FDA Device
- Yes
Countries
- United States
Study Locations
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