Mazor Robotics Receives FDA 510(k) Clearance for Second Generation Renaissance Robotic Spine System

Mazor Robotics’ Renaissance robot for spine surgery has received FDA 510(k) clearance for its new design, interface and next-generation hardware and software, according to a company news release.

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The new system also serves as a platform to support future clinical applications, potentially including robotic-guided cranial surgeries. The company will begin sales immediately.

Read a Reuters report on Mazor’s robotic spine technology.

Related Articles on Spine Technology:
10 Points on Robot-Guided Spine Surgery
Mazor Robotics Receives FDA Clearance for Emerald Spine Implant

5 Spine Clinical Developments to Watch for in 2011

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