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JULY 19, 2017

Radiofrequency Generator Receives FDA 510(k) Clearance

The FDA has granted 510(k) clearance to Stryker’s MultiGen 2 RF Generator for use during radiofrequency ablation, a minimally invasive procedure to relieve facet joint pain.

Procedures are customizable based on patient needs and physician preferences with flexible stimulation controls, according to Stryker. The MultiGen 2 RF Generator will debut at the Spine Intervention Society’s 25th annual meeting July 19-22 in San Francisco.