Tornier Sa

Contact: Jean Claude Crabonneor - VP Marketing & Sales
Web: http://www.tornier.com
Address: 161 Rue Lavoisier, Montbonnot, Saint-Ismier, Cedex F-38330, France
Phone: 33-0-4-76-61-3 | Fax: 33-0-4-76-61-3 | Map/Directions >>

Profile: Tornier Sa offers Non-ceramic metal stem hip prosthesis without self locking ball. Hip prosthesis with acetabular component. Uni-condylar and bi-condylar knee prostheses. Hip bone fixation plate.

The company was founded in 1930, has revenues of USD 5-10 Million, has ~600 employees.

FDA Registration Number: 3000931034
US Agent: Kevin Smith / Tornier Inc.
Phone: +1-(952)-921-7121 Fax: +1-(952)-426-7601 E-Mail:

13 Products/Services (Click for related suppliers)

• Acetabular Mesh Hip Prosthesis (FDA Code: JDJ / 878.3300)

Surgical mesh is a metallic or polymeric screen intended to be implanted to reinforce soft tissue or bone where weakness exists. Examples of surgical mesh are metallic and polymeric mesh for hernia repair, and acetabular and cement restrictor mesh used during orthopedic surgery.

• Bone Fixation Nail (FDA Code: JDS / 888.3030)

Single/multiple component metallic bone fixation appliances and accessories are devices intended to be implanted consisting of one or more metallic components and their metallic fasteners. The devices contain a plate, a nail/plate combination, or a blade/plate combination that are made of alloys, such as cobalt-chromium-molybdenum, stainless steel, and titanium, that are intended to be held in position with fasteners, such as screws and nails, or bolts, nuts, and washers. These devices are used for fixation of fractures of the proximal or distal end of long bones, such as intracapsular, intertrochanteric, intercervical, supracondylar, or condylar fractures of the femur; for fusion of a joint; or for surgical procedures that involve cutting a bone. The devices may be implanted or attached through the skin so that a pulling force (traction) may be applied to the skeletal system.

• Bone Fixation Plate (FDA Code: HRS / 888.3030)

• Condylar Plate Fixation Device Implant (FDA Code: JDP / 888.3030)

• Femoral Trunnion-Bearing Hemi- Hip Prosthesis (FDA Code: JDH / 888.3380)

• Hip Joint Prosthesis

• Metal Cemented Femoral Component Hip Prosthesis (FDA Code: JDG / 888.3360)

A hip joint femoral (hemi-hip) metallic cemented or uncemented prosthesis is a device intended to be implanted to replace a portion of the hip joint. This generic type of device includes prostheses that have a femoral component made of alloys, such as cobalt-chromium-molybdenum. This generic type of device includes designs which are intended to be fixed to the bone with bone cement (888.3027) as well as designs which have large window-like holes in the stem of the device and which are intended for use without bone cement. However, in these latter designs, fixation of the device is not achieved by means of bone ingrowth.

• Metal/Polymer Semi-Constrained Hip Prosthesis (FDA Code: LPH / 888.3358)

A hip joint metal/polymer/metal semi-constrained porous-coated uncemented prosthesis is a device intended to be implanted to replace a hip 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 has a femoral component made of a cobalt-chromium-molybdenum (Co-Cr-Mo) alloy or a titanium-aluminum-vanadium (Ti-6Al-4V) alloy and an acetabular component composed of an ultra-high molecular weight polyethylene articulating bearing surface fixed in a metal shell made of Co-Cr-Mo or Ti-6Al-4V. The femoral stem and acetabular shell have a porous coating made of, in the case of Co-Cr-Mo substrates, beads of the same alloy, and in the case of Ti-6Al-4V substrates, fibers of commercially pure titanium or Ti-6Al-4V alloy. The porous coating has a volume porosity between 30 and 70 percent, an average pore size between 100 and 1,000 microns, interconnecting porosity, and a porous coating thickness between 500 and 1,500 microns. The generic type of device has a design to achieve biological fixation to bone without the use of bone cement.

• Non-Cemented Metal Acetabular Component Hip Prosthesis

• Shoulder joint Prosthesis

• Shoulder Prosthesis

• Spinal Fixation Device Implant (FDA Code: JDN / 888.3060)

A spinal intervertebral body fixation orthosis is a device intended to be implanted made of titanium. It consists of various vertebral plates that are punched into each of a series of vertebral bodies. An eye-type screw is inserted in a hole in the center of each of the plates. A braided cable is threaded through each eye-type screw. The cable is tightened with a tension device and it is fastened or crimped at each eye-type screw. The device is used to apply force to a series of vertebrae to correct "sway back," scoliosis (lateral curvature of the spine), or other conditions.

• Total Shoulder Prosthesis System