Smith & Nephew, Inc.
This registry is designed to collect information on how different surgical procedures are used and how well they work in treating knee cartilage damage. Information will be collected from patients undergoing knee surgery for cartilage damage and entered into a large database that reflects routine clinical practice ("real-world" data). The data collected will be used to support future research and improve understanding of treatment outcomes for knee cartilage repair.
The registry will collect both prospective and retrospective/prospective data.
Inclusion Criteria: Prospective Subjects * Provides written informed consent. * Is eighteen (18) years of age or older at time of consent and considered skeletally mature in the opinion of the investigator. * Scheduled to undergo knee cartilage surgery with the Marketed Product-MP01 OR other knee cartilage repair surgery. * For subjects having other knee cartilage repair surgery: \- Falls within Marketed Product-MP01 on label indication: Knee chondral or osteochondral lesions (ICRS grade III and above, 1-7cm2) in patients with or without mild-moderate knee osteoarthritis (K/L 0-3). * Has…
Marketed Product - MP01 is a medical device used in the treatment of knee-joint surface lesions.
Any other surgical procedures used in the treatment of knee-joint surface lesions that fall within the Marketed Product - MP01 on label indication.
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