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Minute Insight: Stryker And Si-Bone Receive US FDA Clearances For Spine Surgery Guidance System

 
• By Marion Webb

Stryker received FDA 510(k) clearance for its Q Guidance System and Si-Bone received 510(k) clearance for the Granite spinal fusion implant.

Minute Insight
• Source: Informa/Alamy

Two medical device companies, Stryker Corporation and SI-BONE, Inc., announced on 31 May they have received US Food and Drug Administration clearances for devices that increase the success rate of spinal surgery.

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