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Zimmer Biomet Cannulated Screw Systems

The Zimmer Biomet cannulated screw system is a series of cannulated ranging from 3.0 to 8.0 mm. Matching a combination of screw options with necessary instrumentation, the systems provide convenience and flexibility for the orthopaedic surgeon and the OR staff. Consistent with all Zimmer Biomet implants, the screws offer TiMAX® surface treatment which has been shown in mechanical testing, to have increased fatigue strength compared to 316L electropolished stainless steel, type I anodized titanium, and machined titanium.1

The Cannulated Screw System is available in sterile and non-sterile options from 10 mm to 180 mm lengths.

Choice of selection from:

  • 3.0 mm Cannulated Screw– partially threaded, 10-70 mm lengths available (10-40 mm included in tray)
  • 4.0 mm Cannulated Screw – partially and fully threaded,
    10-100 mm lengths available (10-70 mm included in tray)
  • 5.0 mm Cannulated Screw – partially and fully threaded,
    30-100 mm lengths available
  • 6.5 mm Cannulated Screw – 16 mm, 40 mm, and full thread lengths available
    • 16 mm thread: 30 mm – 180 mm lengths available
      (30-125 mm included in tray)
    • 40 mm thread:  70 mm – 180 mm lengths available
      (40-130  mm included in tray)
    • Full thread: 30 mm – 180 mm lengths available
      (30-130 mm included in tray)
  • 8.0 mm Cannulated Screw – 16 mm, 40 mm, and full thread lengths available
    • 16 mm thread: 30 mm – 180 mm lengths available
      (40-130 mm included in tray)
    • 40 mm thread:  70 mm – 180 mm lengths available
    • Full thread: 30 mm – 180 mm lengths available
      (40-130 mm included in tray)

Additional Information

TiMAX Cannulated Screws

1. Zimmer BiometTest # DVA-107504-DVER. Mechanical testing not necessarily indicative of clinical performance. 

 

Legal Manufacturer:                      

Biomet Orthopedics
56 East Bell Drive
P.O. Box 587
Warsaw, Indiana 46581 USA


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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.