Clinical Research Directory

Inclusion Criteria: 1. Patient was treated with the SMR Reverse Shoulder System device (either with 36-mm CoCrMo glenosphere or 40-mm cross-linked UHMWPE glenosphere) between January 1, 2013 and January 1, 2020 as per Instruction for Use 2. Patient was an adult male or female and was 18 years of age or older at the time of surgery 3. Patient received the SMR Reverse Shoulder System for primary, fracture, or revision total shoulder replacement in a grossly rotator cuff deficient joint with severe arthroplasty 4. The patient's joint was anatomically and structurally suited to receive the selected implants, with a functional deltoid muscle 5. Surgery date is at least 24 months from screening of data 6. Patient has baseline radiographs and Oxford Shoulder Score Exclusion Criteria: 1 Patient was treated with the SMR Reverse Shoulder System device (either with 36-mm CoCrMo glenosphere or 40-mm cross-linked UHMWPE glenosphere) between January 1, 2013 and January 1, 2020 out of the Indications for Use