Stryker has received 510(k) clearance from the US Food and Drug Administration (FDA) for its Q Guidance System with Spine Guidance 5 Software featuring Copilot.

This technology is the first on the market to integrate smart-powered instruments into the company’s expanding ecosystem.

Discover B2B Marketing That Performs

Combine business intelligence and editorial excellence to reach engaged professionals across 36 leading media platforms.

Find out more

The Spine Guidance Software with Copilot is designed to support bone resection, pedicle preparation, and screw delivery, providing multiple feedback modalities to optimise a surgeon’s effectiveness and improve patient outcomes.

More than 850 orthopaedic spine surgeons and neurosurgeons collaborated with Stryker to develop this technology.

The software’s Smart Zones offer auditory and sensory feedback to alert surgeons as they approach the planned boundaries of anatomical alert zones with the high-speed drill.

The Copilot Smart Driver complements this feature by automatically stopping at the planned depth, aiding surgeon precision at the time of pedicle preparation and screw placement.

GlobalData Strategic Intelligence

US Tariffs are shifting - will you react or anticipate?

Don’t let policy changes catch you off guard. Stay proactive with real-time data and expert analysis.

By GlobalData

Clinical cases using the Spine Guidance Software with Copilot are set to commence in September 2024.

Stryker is planning for a full commercial launch of the Spine Guidance Software with Copilot later this year.

Stryker spine division president Robbie Robinson said: “Spine Guidance Software with Copilot is just the beginning of our development pipeline.

“While focusing on innovation and the integration of our implants, instrumentation and enabling technologies, we strive to help surgeons perform safe and efficient procedures that enable better patient outcomes.”

Last month, Stryker launched the LIFEPAK 35, its latest product in the monitor / defibrillator space.

Built on an intuitive, modern platform to help advance patient care, the device is designed to support life-saving teams by providing real-time access to critical patient information.

Medical Device Network Excellence Awards - Nominations Closed

Nominations are now closed for the Medical Device Network Excellence Awards. A big thanks to all the organisations that entered – your response has been outstanding, showcasing exceptional innovation, leadership, and impact

Excellence in Action
SC MEDICA’s minimally invasive, radiation free spinal facet fixation system, FFX® is transforming spinal pain management and improving outcomes for surgeons and patients alike. Learn how SC MEDICA’s award-winning technology is redefining standards in facet joint pain treatment.

Discover the Impact