FDA clears Stryker's surgical guidance system

2020 02 20 00 48 1332 Approved Stamp 400

Medical technology developer Stryker has received clearance from the U.S. Food and Drug Administration (FDA) for its Q Guidance System for use in cranial surgeries.

The Q Guidance System is an image-based planning and intraoperative guidance system designed to support cranial surgeries. It tracks instruments and displays their position and orientation in patient image; it also includes algorithmic processing software and guidance data, the company said.

The Q Guidance System was first cleared in September 2022 for spinal applications.

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