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Stryker’s Q Guidance System for cranial applications receives FDA clearance
The Fly

Stryker’s Q Guidance System for cranial applications receives FDA clearance

Stryker announced that its Q Guidance System with Cranial Guidance Software received 510(k) clearance from the U.S. Food and Drug Administration. The Q Guidance System is an image-based planning and intraoperative guidance system designed to support cranial surgeries, the firm says. Recently launched in September 2022, the Q Guidance System for spinal applications is currently available on the market. "The FDA clearance of Stryker’s Q Guidance System with Cranial Guidance Software is a key milestone, which will help lead the transformation of cranial navigation and surgery," said Robbie Robinson, president of Stryker’s Spine division. "Our robust pipeline of iterative launches reinforces our commitment to making industry-leading investments focused on providing advanced navigation products and differentiated technologies that our surgeon customers have come to expect."

Published first on TheFly

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