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iFix® Interference Screw

iFix 7-8mm Notching Screw Driver

iFix 7-8mm Notching Screw Driver

The iFix Interference Screw System was the first self-tapping polyetheretherketone (PEEK) interference screw developed for bone-patellar tendon-bone ACL reconstruction procedures. The interference screws are manufactured using PEEK-OPTIMA®, a non-absorbable polymer that is highly biocompatible, biomechanically strong and radiolucent with decades of proven orthopedic success.  With this material and key design features for easy implementation, this technology provides a solution to surgeons and accommodates all types of pathologies and patient needs with multiple sizes.

iFix 9-12mm Notching Screw Driver

iFix 9-12mm Notching Screw Driver

  • Strong Fixation- Provides high strength for graft fixation
  • Self-Tapping- Advanced design eliminates the need for tapping before insertion, which saves surgeons a step in the procedure
  • Cannulated Driver- Advanced instrumentation is able to lock and slide on guide wire for easy, aligned insertion of screw
  • Radiolucent- Clear post-operative imaging and exceptional image clarity
  • Bio-inert- Ideal modulus that is a close match to bone modulus to minimize stress-shielding and provide for a healing environment

Additional Information

PEEK-OPTIMA® is a registered trademark of Invibio Limited.

Legal Manufacturer:

Cayenne Medical, a Zimmer Biomet Company
16597 North 92nd Street Suite 101
Scottsdale, AZ 85260 USA

All content herein is protected by copyright, trademarks and other intellectual property rights, as applicable, owned by or licensed to Zimmer Biomet or its affiliates unless otherwise indicated, and must not be redistributed, duplicated or disclosed, in whole or in part, without the express written consent of Zimmer Biomet.  
This material is intended for health care professionals. Distribution to any other recipient is prohibited.
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.