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(shoulder(s), arm(s)).\n* Subjects with prior shoulder surgery on index shoulder, including subacromial decompression, biceps tenodesis\u002Ftenotomy, and acromioclavicular joint (ACJ) excision\u002Fdistal clavicle excision (DCE).\n* Subjects with a planned surgery on the contra-lateral shoulder within the study period.\n* Systemic steroid use (oral, IV) or local steroid injection within 3 months of the date of surgery.\n* Subjects with a full thickness rotator cuff tear.\n* Subjects with a subscapularis tear requiring repair.\n* Subjects requiring a concomitant labral fixation procedure, concomitant surgery for bone defects requiring bone implantation or for superior labral tear from anterior to posterior (SLAP).\n* Subjects requiring a concomitant os acromiale fixation procedure.\n* Subjects with glenohumeral joint instability (multiple dislocations\u002Fsubluxations).\n* Subjects with condition(s) that contraindicate or complicate outcomes of Isolated Bioinductive Repair or completion and repair e.g., \\> Hamada 3 rotator cuff arthropathy on X-ray, Goutallier atrophy \\> Grade 3, proximal humeral fracture or scapular fracture, avascular necrosis of the humeral head.\n* Subjects with neurologic conditions effecting either upper extremity.\n* Subjects who are unable to tolerate magnetic resonance imaging (MRI), due to psychiatric or medical contraindications.\n* Subjects who are pregnant or breast feeding.\n* Subjects who are currently involved in any injury litigation relating to the index shoulder.\n* Subjects with current workers compensation claim.\n* Subjects who are enrolled, or plan to enroll, in another clinical trial during this study that would affect the outcomes of this study.\n* Subjects with a history of poor compliance with medical treatment, physical therapy (PT)\u002Frehabilitation, or clinical study participation.\n* Subject who, in the opinion of the Investigator, has an emotional or neurological condition that would pre-empt their 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