Pilot Study of Augment Rotator Cuff for Surgical Treatment of Full Thickness Rotator Cuff Tears

Exclusion Criteria

• •The subject has undergone previous rotator cuff repair surgery to the affected shoulder
• •The subject has a partial thickness rotator cuff tear
• •The subject requires a concomitant subscapularis repair
• •The subject requires a concomitant labral repair
• •The subject has an irreparable rotator cuff tear
• •The subject has an allergy to yeast-derived products or a known bovine collagen allergy
• •The subject has implanted metallic devices (cardiac pacemakers, insulin pumps, and nerve stimulators), medically implanted clips or other electronically, magnetically or mechanically activated implants that would contraindicate undergoing an MRI scan of the shoulder
• •The subject has tested positive or has been treated for a malignancy in the past or is suspected of having a malignancy or is currently undergoing radiation or chemotherapy treatment for a malignancy anywhere in the body, whether adjacent to or distant from the proposed Augment Rotator Cuff implantation site
• •The subject's condition represents a worker's compensation case
• •The subject is currently involved in a health-related litigation procedure
• •The subject is pregnant or able to become pregnant but not practicing a medically-accepted form of birth control, and/or intending to become pregnant during this study period