SCORPIO CRUCIATE RETAINING (CR) TIBIAL INSERT - Prosthesis, knee, internal, insert component Australia - English - Department of Health (Therapeutic Goods Administration)

scorpio cruciate retaining (cr) tibial insert - prosthesis, knee, internal, insert component

stryker australia pty ltd - 46585 - prosthesis, knee, internal, insert component - the cruciate retaining tibial insert is assembled intra-operatively to the tibial tray. it is a standard non-constrained bearing surface made of ultra high molecular weight polyethylene (uhmwpe) and is used only with the cr femoral component. a device used to repair or replace the tibial plateau of the knee joint. indications: painful, disabling joint disease of the knee resulting from: degenerative arthritis, rheumatoid arthritis or post-traumatic arthritis. post-traumatic loss of knee joint configuration and function. moderate varus, valgus, or flexion deformity in which the ligamentous structures can be returned to adequate function and stability. revision of previous unsuccessful knee replacement or other procedure.

Scorpio HA Tibial Tray - Coated knee tibia prosthesis Australia - English - Department of Health (Therapeutic Goods Administration)

scorpio ha tibial tray - coated knee tibia prosthesis

stryker australia pty ltd - 34198 - coated knee tibia prosthesis - this total knee system includes femoral, patella, tibial tray, tibal bearing and bone augmentation components which are designed to be used together to achieve total reconstructive replacement of the knee joint. these tibial tray components are permanently implantable and are available in various sizes to address varying patient and surgeon requirements for primary and revision applications. all devices feature a coating of ha on their external surface to encourage bone in growth. a total knee implant intended to be used in primary or revision joint arthroplasty of the knee. indications for use of total knee replacement include: painful, disabling joint disease of the knee resulting from: degenerative arthritis, rheumatoid arthritis or post-traumatic arthritis. post-traumatic loss of knee joint configuration and function. moderate varus, valgus, or flexion deformity in which the ligamentous structures can be returned to adequate function and stability. revision of previous unsuccessful knee replacement or oth

SCORPIO TOTAL STABILISER (TS) TIBIAL INSERT - Prosthesis, knee, internal, insert component Australia - English - Department of Health (Therapeutic Goods Administration)

scorpio total stabiliser (ts) tibial insert - prosthesis, knee, internal, insert component

stryker australia pty ltd - 46585 - prosthesis, knee, internal, insert component - the total stabilised tibial bearing insert is assembled intra-operatively to the tibial tray. it has a raised tibial eminence designed for increased anterior/posterior constraint, resistance to posterior subluxation, and varus/valgus stability. and is made of ultra high molecular weight polyethylene (uhmwpe). it is package with a reinforcing pin and is for use only with ts femoral components. a device used to repair or replace the tibial plateau of the knee joint. indications: painful, disabling joint disease of the knee resulting from: degenerative arthritis, rheumatoid arthritis or post-traumatic arthritis. post-traumatic loss of knee joint configuration and function. moderate varus, valgus, or flexion deformity in which the ligamentous structures can be returned to adequate function and stability. revision of previous unsuccessful knee replacement or other procedure. ts components only: severe anteroposterior and medial/lateral instability of the knee joint.

SCORPIO TOTAL STABILISER (TS) WAFFLE, TIBIAL TRAY - Uncoated knee tibia prosthesis, metallic Australia - English - Department of Health (Therapeutic Goods Administration)

scorpio total stabiliser (ts) waffle, tibial tray - uncoated knee tibia prosthesis, metallic

stryker australia pty ltd - 32832 - uncoated knee tibia prosthesis, metallic - the ts design of the tibial component has raised tibial eminence designed for increased anterior/posterior constraint, resistance to posterior subluxation and varus/valgus stability. the tibial tray is made of cobalt chromium alloy and is packaged together with a cocr cap screw and is intended to be used with cement. a device used to repair or replace the tibial plateau of the knee joint. indications: painful, disabling joint disease of the knee resulting from: degenerative arthritis, rheumatoid arthritis or post-traumatic arthritis. post-traumatic loss of knee joint configuration and function. moderate varus, valgus, or flexion deformity in which the ligamentous structures can be returned to adequate function and stability. revision of previous unsuccessful knee replacement or other procedure. ts components only: severe anteroposterior and medial/lateral instability of the knee joint.

Series 7000 Tibial Tray w/PA - Coated knee tibia prosthesis Australia - English - Department of Health (Therapeutic Goods Administration)

series 7000 tibial tray w/pa - coated knee tibia prosthesis

stryker australia pty ltd - 34198 - coated knee tibia prosthesis - this total knee system includes femoral, patella, tibial tray, tibal bearing and bone augmentation components which are designed to be used together to achieve total reconstructive replacement of the knee joint. these tibial tray components are permanently implantable and are available in various sizes to address varying patient and surgeon requirements for primary and revision applications. all devices feature a coating of pa on their external surface to encourage bone in growth. total knee implant used in primary or revision joint arthroplasty of the knee indications include:painful, disabling joint disease of the knee resulting from: degenerative arthritis, rheumatoid arthritis or post-traumatic arthritis. post-traumatic loss of knee joint configuration and function. moderate varus, valgus, or flexion deformity in which the ligamentous structures can be returned to adequate function and stability. revision of previous unsuccessful knee replacement or other procedure.

Sigma RP-F Tibial Inserts - Prosthesis, knee, internal, insert component Australia - English - Department of Health (Therapeutic Goods Administration)

sigma rp-f tibial inserts - prosthesis, knee, internal, insert component

johnson & johnson medical pty ltd t/a depuy synthes - 46585 - prosthesis, knee, internal, insert component - the sigma rp-f tibial inserts are manufactured from uhmwpe and reinforced with astm f-90 co-cr-mo alloy pins. the sigma rp-f tibial inserts articulate with the sigma rp-f femoral component and m.b.t. primary and revision trays. the sigma rp-f tibial inserts are part of the lcs complete ? p.f.c. sigma rp mobile bearing total knee system and are indicated for use in cases of osteoarthritis and rheumatoid arthritis. the sigma rp-f inserts are indicated where a higher than normal degree of post-operative flexion is required.

Triathlon Beaded Tibial Baseplates w/ PA - Coated knee tibia prosthesis Australia - English - Department of Health (Therapeutic Goods Administration)

triathlon beaded tibial baseplates w/ pa - coated knee tibia prosthesis

stryker australia pty ltd - 34198 - coated knee tibia prosthesis - this total knee system includes femoral, patella, tibial tray, tibal bearing and bone augmentation components which are designed to be used together to achieve total reconstructive replacement of the knee joint. these tibial tray components are permanently implantable and are available in various sizes to address varying patient and surgeon requirements for primary and revision applications. all devices feature a coating of pa on their external surface to encourage bone in growth. a beaded tibial baseplate with pa coating component as part of the triathlon total knee system intended for total knee arthroplasty (tka). indications include: painful, disabling joint disease of the knee resulting from noninflammatory degenerative joint disease; and moderate varus, valgus, or flexion deformity in which the ligamentous structures can be returned to adequate function and stability.

e.motion UC Meniscal Component with tibial pivot  - Mobile-bearing total knee prosthesis Australia - English - Department of Health (Therapeutic Goods Administration)

e.motion uc meniscal component with tibial pivot - mobile-bearing total knee prosthesis

b braun australia pty ltd - 32841 - mobile-bearing total knee prosthesis - e.motion? uc meniscal component is a rotating meniscal component whose ultra-congruent design aims for mobility and stability. e.motion? uc allows the surgeons the intraoperative choice to either preserve or substitute the posterior cruciate ligament. functioning collateral ligaments, balances joint gaps and the highly congruent prosthesis design allow resecting the pcl without femoral bone loss. the device is made from polyethylene with x-ray markers and includes a cocrmo tibial pivot. the implant is a component of the e.motion? system which is indicated for patients requiring primary or revision surgery. it is used as a component part of a human knee endoprosthesis in combination with e.motion mobile bearing knee endoprosthetic components. indications: severe knee joint conditions that cannot be treated through other therapies: - degenerative osteoarthritis - rheumatoid arthritis - posttraumatic arthritis - symptomatic knee instability - knee stiffness - deformation of the knee joint the surgeon can select the optimum solution for the patient from the various implant types of the knee systems, according to the severity of the condition. the surgeon is responsible for correctly establishing the indication.

e.motion PS Meniscal Component with tibial pivot - Mobile-bearing total knee prosthesis Australia - English - Department of Health (Therapeutic Goods Administration)

e.motion ps meniscal component with tibial pivot - mobile-bearing total knee prosthesis

b braun australia pty ltd - 32841 - mobile-bearing total knee prosthesis - e.motion? ps meniscal component is a posterior stabilised mobile bearing insert that allows free axial rotation, for easier mobility of the joint through the entire range of movement and uniform load distribution. the device is made from polyethylene with x-ray markers and includes a cocrmo tibial pivot. the implant is a component of the e.motion? system which is indicated for patients requiring primary or revision surgery. it is used as a component part of a human knee endoprosthesis in combination with e.motion mobile bearing knee endoprosthetic components. indications: severe knee joint conditions that cannot be treated through other therapies: - degenerative osteoarthritis - rheumatoid arthritis - posttraumatic arthritis - symptomatic knee instability - knee stiffness - deformation of the knee joint the surgeon can select the optimum solution for the patient from the various implant types of the knee systems, according to the severity of the condition. the surgeon is responsible for correctly establishing the indication.

Vanguard DA360 Tibial Tray - Uncoated knee tibia prosthesis, metallic Australia - English - Department of Health (Therapeutic Goods Administration)

vanguard da360 tibial tray - uncoated knee tibia prosthesis, metallic

zimmer biomet pty ltd - 32832 - uncoated knee tibia prosthesis, metallic - cobalt chrome alloy tibial tray is for cemented use features 25 mm tapered stem boss which accepts offset stem adapters, stem extensions and cruciate wing augments. the superior surface features a cylindrical post that blends into a distal cone which is designed to mate with the vanguard da 360 tibial bearing. the seven symmetrical baseplate sizes in 4 mm m/l increments. packaged with ti/uhmwpe screw. cobalt chrome alloy tibial tray is a component of vanguard ssk 360 revision knee system. indications for use: painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, traumatic arthritis where one or more compartments are involved; correction of varus, valgus, or posttraumatic deformity; correction or revision of unsuccessful osteotomy, arthrodesis, or failure of previous joint replacement procedure.