Australia - English - Department of Health (Therapeutic Goods Administration)

adler ortho australia pty ltd - 34198 - coated knee tibia prosthesis - ti6al4v with porous titanium & ha coating. a fixed-bearing tibial component showing a non-anatomical shape and a keel to be anchored to the bone. keel features 2 delta-shaped wings. central part is truncated cone-shaped to anchor tibial stems. locking system for tibial insert - step to be coupled to flexible clips located in the anterior part of tibial insert; posterior part, stair to be coupled with a groove located at the base of tibial insert avoids detachment of components. a tibial component of a tricompartmental fixed-bearing prosthesis to be used in pcl (posterior cruciate ligament) retaining/sacrificing tkr (total knee replacement) for primary and revision surgery. main indications: - primary and secondary arthrosis - rheumatoid arthritis - bone necrosis - revisions, where other devices or treatments have failed

Australia - English - Department of Health (Therapeutic Goods Administration)

adler ortho australia pty ltd - 32832 - uncoated knee tibia prosthesis, metallic - composed of ti6al4v. a fixed-bearing tibial component showing a non-anatomical shape and a keel to be anchored to the bone with bone cement. keel features two delta-shaped wings. central part is truncated cone-shaped, to anchor tibial stems. locking system for tibial insert - a step to be coupled to flexible clips located in the anterior part of the tibial insert; posterior part, a stair to be coupled with a groove located at the base of the tibial insert avoids detachment of the components. a tibial component of a tricompartmental fixed-bearing prosthesis to be used in pcl (posterior cruciate ligament) retaining/sacrificing tkr (total knee replacement) for primary and revision surgery. main indications: - primary and secondary arthrosis - rheumatoid arthritis - bone necrosis - revisions, where other devices or treatments have failed

Australia - English - Department of Health (Therapeutic Goods Administration)

adler ortho australia pty ltd - 33745 - coated knee femur prosthesis - composed of cocrmo alloy coated with layers of sintered cocrmo beads and ha. a posterior stabilized femoral component of a total knee replacement prosthesis for pcl (posterior cruciate ligament) sacrificing. multi-radius femoral design for cementless fixation. between the two condyles, a cam is located. the mechanical interaction between the cam and the post located on the tibial insert allows the roll-back mechanism to occur. post and cam have been designed in order to minimize shear stresses a femoral component of a tricompartmental rotating platform prosthesis to be used in pcl (posterior cruciate ligament) sacrificing tkr (total knee replacement) for primary and revision surgery. main indications: - primary and secondary arthrosis - rheumatoid arthritis - bone necrosis - revisions, where other devices or treatments have failed

Australia - English - Department of Health (Therapeutic Goods Administration)

adler ortho australia pty ltd - 32831 - uncoated knee femur prosthesis - composed of cocrmo alloy. a posterior stabilized femoral component of a total knee replacement prosthesis for pcl (posterior cruciate ligament) sacrificing. multi-radius femoral design. between the two condyles, a cam is located. the mechanical interaction between the cam and the post located on the tibial insert allows the roll-back mechanism to occur. post and cam have been designed in order to minimize shear stresses. to be fixed with bone cement. a femoral component of a tricompartmental rotating platform prosthesis to be used in pcl (posterior cruciate ligament) sacrificing tkr (total knee replacement) for primary and revision surgery. main indications: - primary and secondary arthrosis - rheumatoid arthritis - bone necrosis - revisions, where other devices or treatments have failed

Australia - English - Department of Health (Therapeutic Goods Administration)

adler ortho australia pty ltd - 48069 - uncoated unicondylar knee tibia prosthesis, polyethylene - a cemented single-piece all-poly tibial component of a unicompartmental knee replacement prosthesis composed of uhmw-pe. anterior chamfer to avoid potential patellar conflicts. flat articular surface to facilitate a linear contact with the condyle and better distribute the loading forces. a cemented single-piece tibial component of a medial unicompartmental knee replacement prosthesis. indicated when; ? medial compartment osteoarthritis or avascular necrosis with a well-preserved lateral compartment presenting an intact meniscus and full thickness cartilage. ? normally functioning anterior and posterior cruciate ligaments ? varus deformity able to be passively corrected and in any case lower than 15?. ? flexion contracture less than 15?. ? patello-femoral arthritis is not considered a contraindication. ? age, weight and patient activity level are not considered a contraindication for unicompartmental knee replacement.

Australia - English - Department of Health (Therapeutic Goods Administration)

adler ortho australia pty ltd - 48070 - unicondylar knee insert - a tibial insert component of a unicompartmental knee replacement prosthesis composed of uhmw-pe. anterior chamfer to avoid potential patellar conflicts. outer edge rounded to cover the metal back, to avoid potential conflicts between metal and soft parts. flat articular surface to facilitate a linear contact with the condyle and better distribute the loading forces. a tibial insert component of a medial unicompartmental knee replacement prosthesis. indicated when; ? medial compartment osteoarthritis or avascular necrosis with a well-preserved lateral compartment presenting an intact meniscus and full thickness cartilage. ? normally functioning anterior and posterior cruciate ligaments. ? varus deformity able to be passively corrected and in any case lower than 15?. ? flexion contracture less than 15?. ? patello-femoral arthritis is not considered a contraindication. ? age, weight and patient activity level are not considered a contraindication for unicompartmental knee replacement.

Australia - English - Department of Health (Therapeutic Goods Administration)

adler ortho australia pty ltd - 48065 - coated unicondylar knee tibia prosthesis - a cementless ti6al4v alloy tibial component of a unicompartmental knee replacement prosthesis with 3d ti-por monolithic surface + ha coating. the shape & dimensions of the tibial component have been designed to adapt to the medial & lateral compartment, maximizing contact with the peripheral cortical bone. dovetail implant blocking system to minimise micro-movements. mirror finish & stabilization keel to contrast varus/valgus stress. anchoring pin for primary stabilization of the tibial tray. a cementless tibial component of a medial unicompartmental knee replacement prosthesis. indicated when; ? medial compartment osteoarthritis or avascular necrosis with a well-preserved lateral compartment presenting an intact meniscus and full thickness cartilage. ? normally functioning anterior and posterior cruciate ligaments. ? varus deformity able to be passively corrected and in any case lower than 15?. ? flexion contracture less than 15?. ? patello-femoral arthritis is not considered a contraindication. ? age, weight and patient activity level are not considered a contraindication for unicompartmental knee replacement.

Australia - English - Department of Health (Therapeutic Goods Administration)

adler ortho australia pty ltd - 48068 - uncoated unicondylar knee tibia prosthesis, metallic - a cemented ti6al4v alloy tibial component of a unicompartmental knee replacement prosthesis. the shape and dimensions of the tibial component have been designed to adapt to both the medial and lateral compartment, maximizing the contact with the peripheral cortical bone. dovetail implant blocking system to minimise micro-movements. mirror finish and stabilization keel to contrast varus / valgus stress. anchoring pin for primary stabilization of the tibial tray. a cemented tibial component of a medial unicompartmental knee replacement prosthesis. indicated when; ? medial compartment osteoarthritis or avascular necrosis with a well-preserved lateral compartment presenting an intact meniscus and full thickness cartilage. ? normally functioning anterior and posterior cruciate ligaments. ? varus deformity able to be passively corrected and in any case lower than 15?. ? flexion contracture less than 15?. ? patello-femoral arthritis is not considered a contraindication. ? age, weight and patient activity level are not considered a contraindication for unicompartmental knee replacement.

Australia - English - Department of Health (Therapeutic Goods Administration)

adler ortho australia pty ltd - 34209 - coated unicondylar knee femur prosthesis - a cementless cocrmo alloy femoral component of a unicompartmental knee replacement prosthesis with 3d co-por monolithic surface + ha coating. 6mm constant thickness of the implant. rotation center at constant radius of flexion from 0 to 90 degrees. the 3-degree closure of the posterior condyle increases the range of motion and the stability of the system. external distal apex blunted. optimizes m/l positioning without risk of protrusion. outer edge with softened radius. a cementless femoral component of a medial unicompartmental knee replacement prosthesis. indicated when; ? medial compartment osteoarthritis or avascular necrosis with a well-preserved lateral compartment presenting an intact meniscus and full thickness cartilage. ? normally functioning anterior and posterior cruciate ligaments. ? varus deformity able to be passively corrected and in any case lower than 15?. ? flexion contracture less than 15?. ? patello-femoral arthritis is not considered a contraindication. ? age, weight and patient activity level are not considered a contraindication for unicompartmental knee replacement.

Australia - English - Department of Health (Therapeutic Goods Administration)

adler ortho australia pty ltd - 33369 - uncoated unicondylar knee femur prosthesis - a cemented femoral component of a unicompartmental knee replacement prosthesis composed of cocrmo alloy. 6mm constant thickness of the implant. rotation center at constant radius of flexion from 0 to 90 degrees. the 3-degree closure of the posterior condyle increases the range of motion and the stability of the system. external distal apex blunted. optimizes m/l positioning without risk of protrusion. outer edge with softened radius. a cemented femoral component of a medial unicompartmental knee replacement prosthesis. indicated when; ? medial compartment osteoarthritis or avascular necrosis with a well-preserved lateral compartment presenting an intact meniscus and full thickness cartilage. ? normally functioning anterior and posterior cruciate ligaments. ? varus deformity able to be passively corrected and in any case lower than 15?. ? flexion contracture less than 15?. ? patello-femoral arthritis is not considered a contraindication. ? age, weight and patient activity level are not considered a contraindication for unicompartmental knee replacement.