Stryker earns FDA clearance for cranial guidance system

Medical technology company Stryker has earned 510(k) FDA clearance for its Q Guidance System with Cranial Guidance Software. 

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The Q Guidance System launched in September 2022 for spinal applications and is currently available on the market. With the new software, the guidance system can support cranial procedures as well. 

The cranial guidance system, powered by Stryker’s Q guidance technology, can be used with a wide range of instruments and accessories for cranial navigation, according to a Feb. 17 press release. 

The new software is cleared for any procedure in which computer-assisted planning and surgery is appropriate. 

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