Activ Screw
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Ø6.5 mm cannulated and compression screws.

The implants in the Stand-Alone Screws range are designed for the fixation of fractures, osteotomies and bone arthrodesis in adults, appropriate to the size of the device.

The Activ Screw range consists of three compressive Ø6.5 mm cannulated hexalobe screws, one with a long thread, one with a short thread and a fully threaded positioning screw. An intuitive and specific kit has been designed to insert these screws.

Our philosophy.

SHORT THREAD COMPRESSION SCREW

The Ø6.5 mm compression screws with a short thread of 16 mm, available in lengths from 40 mm to 120 mm, are guided in a straight line along a 2.5 mm diameter pin thanks to their cannulation.

These screws are not available in the Activ Screw kit; they are available separately in single-unit sterile packaging (S-box).

LONG THREAD COMPRESSION SCREW

The Ø6.5 mm compression screws with a 32 mm long thread, available in lengths from 45 to 120 mm, are guided in a straight line along a 2.5 mm diameter pin thanks to their cannulation.

These screws are not available in the Activ Screw kit; they are available separately in single-unit sterile packaging (S-box).

POSITIONING SCREW

The Ø6.5 mm positioning screws with full thread, available in lengths from 40 mm to 120 mm, are guided in a straight line along a 2.5 mm diameter pin thanks to their cannulation.

These screws are not available in the Activ Screw kit; they are available separately in single-unit sterile packaging (S-box).

The key features of the Activ Screw range.

  • Three models of cannulated screws: short-thread compression, long-thread compression and positioning screw
  • T25 hexalobe format
  • Complete and intuitive instrumentation kit
  • Protective drill guide allowing minimally invasive surgery while securing the surrounding soft tissues
  • Two types of screwdriver handles available for screwing: T-handle and straight handle

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The purpose of this information is to present the Newclip Technics range of medical devices. These products must be handled and/or implanted by trained and qualified personnel who have read the instructions for use. The surgeon remains responsible for his or her own professional and clinical judgement prior to the use of specific products on a given patient.