Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Stryker Orthopaedics
Age
Any age
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Subject is a candidate for a revision of a failed acetabular component with the Restoration Anatomic Acetabular Shell.
Subject has signed an IRB-approved, study specific Informed Consent Form (ICF).
Subject is skeletally mature.
Subject is a male or non-pregnant female.
Subject is willing and able to comply with postoperative scheduled clinical evaluations.
You may not be if
Subject has a non-Stryker retained stem at the time of study device implantation.
Subject has a Body Mass Index (BMI) \> 45.
Subject has an active or suspected latent infection in or about the affected hip joint at time of study device implantation.
Subject has a mental or neuromuscular disorder which would create an unacceptable risk of prosthesis instability, prosthesis fixation failure, or complications in postoperative care.
Subject has compromised bone stock which cannot provide adequate support and/or fixation to the prosthesis.
Subject is diagnosed with a systemic disease (e.g. Lupus Erythematosus) or a metabolic disorder (e.g. Paget's Disease) leading to progressive bone deterioration.
Subject is immunologically suppressed or receiving steroids in an excess of normal physiological requirements (e.g. \> 30 days).
Subject has a known sensitivity to device materials.
Subject is a prisoner.
Clareo Health | Restoration Anatomic Acetabular Shell Revision Study
