The REDAPT Porous Augments are indicated for:
- Hip components are indicated for patients undergoing primary and revision surgery, when other therapies or devices have failed to restore hip function, following injury or non-inflammatory degenerative joint disease (NIDJD) or any of its composite diagnoses, including osteoarthritis, avascular necrosis, traumatic arthritis, slipped capital epiphysis, fused hip, fracture of the pelvis and diastrophic variant.
- Hip components are also recommended for those with congenital dysplasia, inflammatory degenerative joint disease, such as rheumatoid arthritis and arthritis, brought on by a number of other illnesses and defects.
- Treatment of proximal femur trochanteric fractures, with head involvement, femoral neck fractures
- Girdlestone resection, femoral osteotomy, or endoprosthesis nonunion, that cannot be managed with conventional methods.
- Hip fracture-dislocation surgery and deformity repair.
REDAPT Augments should only be used once and should be implanted with bone cement to the acetabular shell, that they are meant to fit into and without bone cement to the bone interface. When the acetabulum exhibits deficits in the acetabular roof, anterior or posterior pillar, medial wall deficiency and/or protrusion as a result of the causes previously described, augmentations are intended to be employed in main and revision procedures.
