Global Manufacturing Technology Pty Ltd.

Contact: Rick Luccini
Address: 8 Resolution Drive, Unanderra, Wollongong, New South Wales 2526, Australia
Phone: +61-(2)-427-24493 | Map/Directions >>

Profile: Global Manufacturing Technology Pty Ltd. supplies a range of knee prosthesis. Our products include semi-constrained femorotibial knee prosthesis and semi-constrained parallelogram knee prosthesis.

FDA Registration Number: 3004537778
US Agent: Rene Van De Zande / Emergo Global Representation Llc
Phone: +1-(512)-327-9997 Fax: +1-(512)-327-9998 E-Mail:

2 Products/Services (Click for related suppliers)

• Semi-Constrained Femorotibial Knee Prosthesis (FDA Code: HRY / 888.3530)

A knee joint femorotibial metal/polymer semi-constrained cemented prosthesis is a device intended to be implanted to replace part of a knee joint. The device limits translation and rotation in one or more planes via the geometry of its articulating surfaces. It has no linkage across-the-joint. This generic type of device includes prostheses that consist of a femoral component made of alloys, such as cobalt-chromium-molybdenum, and a tibial component made of ultra-high molecular weight polyethylene and is limited to those prostheses intended for use with bone cement (888.3027).

• Semi-Constrained Patellofemoral Knee Prosthesis (FDA Code: KRR / 888.3540)

A knee joint patellofemoral polymer/metal semi-constrained cemented prosthesis is a two-part device intended to be implanted to replace part of a knee joint in the treatment of primary patellofemoral arthritis or chondromalacia. The device limits translation and rotation in one or more planes via the geometry of its articulating surfaces. It has no linkage across-the-joint. This generic type of device includes a component made of alloys, such as cobalt-chromium-molybdenum or austenitic steel, for resurfacing the intercondylar groove (femoral sulcus) on the anterior aspect of the distal femur, and a patellar component made of ultra-high molecular weight polyethylene. This generic type of device is limited to those devices intended for use with bone cement (888.3027). The patellar component is designed to be implanted only with its femoral component.