ZMR® Hip System

A mid-stem modular junction allows for the selection of a proximal body design independent of the choice for a distal stem design. The mid-stem design also allows for completely independent proximal/distal implant positioning and component sizing. This enables a wide variety of bone conditions to be accommodated that are often not fully revealed until the time of surgery. ZMR Implants are available in either a standard junction design or with an extra large junction (XL junction) for larger patients or for those patients whose femur may not provide adequate proximal support.

The system also accommodates a number of fixation philosophies, including distal fixation, proximal fixation, and extensive porous fixation.

The ZMR Hip System includes three distinct porous body styles.

Straight and bowed spline stems are available in up to three stem lengths, in six diameters, to optimize patient fit. The coronal slot makes the distal stem more flexible, allowing for easier stem insertion.

Straight and bowed porous stems are available in up to three stem lengths, in eight diameters, to optimize patient fit. The Porous Stems are coated with plasma-sprayed Tivanium® 6Al-4V Alloy to allow for biological fixation.

The corundumized, splined taper stem is designed to provide distal fixation that transmits axial, torsional, and bending loads to the adjacent bone.

Please refer to the package inserts for complete product information, including contraindications, warnings, precautions, and adverse effects.

Indications

The ZMR Hip Prosthesis is indicated for cementless total hip arthroplasty in patients whose bone stock is of poor quality or inadequate for other reconstruction techniques as indicated by deficiencies of the femoral head, neck or portions of the proximal femur. Arthroplasty should be performed only when more conservative methods of treatment have failed to provide symptomatic relief or when there is progressive disability.

Contraindications

Contraindications include: 

  • Use of this device when a less invasive procedure would be sufficient
  • Skeletal immaturity
  • Loss of abductor musculature in the affected limb
  • Poor bone stock (e.g., steroid-induced metabolic bone disease)
  • Poor skin coverage around the hip joint
  • Neuromuscular disease (e.g., Charcot’s joint) in the affected limb

Additional Information

Legal Manufacturer:

Zimmer, Inc.
1800 West Center Street
Warsaw, Indiana 46580 USA


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For product information, including indications, contraindications, warnings, precautions, potential adverse effects and patient counseling information, see the package insert and information on this website. To obtain a copy of the current Instructions for Use (IFU) for full prescribing and risk information, please call 1-800-348-2759, press 4 for 411 Technical Support.