Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Smith & Nephew, Inc.
Age
21–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Subjects with grossly deficient rotator cuff with severe arthropathy or Subjects with failed joint replacement with grossly deficient rotator cuff
Subjects with a shoulder joint anatomically and structurally suited to receive the device
Subjects at least 21 years of age and skeletally mature at the time of surgery
Subject provided consent to participate in the clinical study (having signed the Informed Consent Form)
You may not be if
Subjects without a functional deltoid muscle
Subjects with active local or systemic infection
Subjects with inadequate bone stock in the proximal humerus or glenoid fossa for supporting the components
Subjects with poor bone quality such as osteoporosis where there could be considerable migration of the prosthesis and/or a chance of fracture of the humerus or glenoid
Subjects with muscular, neurologic, or vascular deficiencies that compromise the affected extremity
Subjects with known metal allergies
Subjects are known to be at risk for lost to follow-up, or failure to return for scheduled visits
Subjects who are prisoners
Female subject who are pregnant, nursing, or of childbearing potential while not practicing effective contraceptive methods
