ZMR® Femoral Revision 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 femoral bone conditions to be accommodated that are often not fully revealed until the time of surgery. The modular proximal bodies and distal stems provide many sizing options to help achieve anatomic restoration.

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 have adequate proximal support. The ZMR XL Hip System was specifically designed to accommodate cases in which proximal support is not obtainable with the standard junction components. 

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

Indications

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
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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.