Australija - engleski - 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

Australija - engleski - 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

Australija - engleski - Department of Health (Therapeutic Goods Administration)

adler ortho australia pty ltd - 46585 - prosthesis, knee, internal, insert component - composed of uhmw-pe. posterior cruciate ligament sacrificing mobile bearing insert, with a central pivot to be coupled to the hole of the tibial component, so that rotation can occur. post on the central part of the articular surface. mechanical interaction between the post and the cam of the genus ps femoral component allows the roll-back mechanism to occur, avoiding the anterior luxation of the insert. post and cam show the same radius of curvature, so that shear stress can be minimized. a tibial insert 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

Australija - engleski - Department of Health (Therapeutic Goods Administration)

adler ortho australia pty ltd - 34198 - coated knee tibia prosthesis - constructed from cocrmo-powder manufactured alloy with porous surface & ha coating. features a non-anatomical shape and a posterior recess to allow retention of the pcl. contains a central hole designed to receive the central pivot of the mobile bearing platform, allowing rotational motion to occur. designed with a delta-shaped keel. the bone fixation of the genus tibial trays can be improved using tibial keel enlargements or extension stems, with or without offset connections. a tibial component of a tricompartmental mobile-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

Australija - engleski - Department of Health (Therapeutic Goods Administration)

adler ortho australia pty ltd - 46585 - prosthesis, knee, internal, insert component - composed of uhmw-pe. non-anatomical, posterior stabilized fixed bearing tibial insert designed to allow the pcl to be removed. tibio-femoral articular surface featuring an ap radius not completely congruent with the ap radius of the ps femoral component. locking system for fixation to the genus tibial tray fb; 2 flexible clips in the anterior part of the insert couple the insert with the tibial tray. couples to the tibial tray with a groove to avoid detachment of the components a tibial insert component of a tricompartmental fixed-bearing 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

Australija - engleski - Department of Health (Therapeutic Goods Administration)

adler ortho australia pty ltd - 59688 - femoral head/stem prosthesis adaptor - the modula neck is manufactured from titanium alloy. the modula? system allows for the independent adjustment of the 3 main parameters: length, offset, version. the 27 points of the tridimensional matrix are covered with the 15 different necks. by combining the matrix positions with the three head options available, the surgeon has 81 different options at his disposal to accurately reconstruct the hip joint geometry. to be used to replace the femoral neck as part of a hip replacement prosthesis. to optimize the reciprocal position of the stem and cup on the basis of the articular needs of the patient, by restoring the physiological offset and length. indicated for use in; primary and secondary arthrosis; rheumatoid and degenerative arthritis, deformities, such as dysplasia; fractures and necrosis of bone; revisions, where other devices or treatments have failed; metastatic diseases

Australija - engleski - 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.

Australija - engleski - 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.

Australija - engleski - 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.

Australija - engleski - 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.