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Stryker receives FDA 510(k) clearance for MultiGen 2 RF Generator
Stryker recently announced it has received FDA 510(k) clearance for its MultiGen 2 RF Generator to be used for radiofrequency ablation.
According to a company press release, the MultiGen 2 RF Generator provides increased reliability and efficiency by achieving target temperature faster and with fewer errors. The release also noted the generator maximizes time and schedules by creating strip lesions without removing electrodes and resolves errors without stopping the procedure. Flexible stimulation controls allow for customizable procedures based on patient needs and physician preferences.
“The next generation of radiofrequency ablation has arrived,” Brad Wallace, brand manager for Stryker, said in the release. “The MultiGen 2 RF Generator provides physicians with control and confidence, making radiofrequency ablation more efficient and reliable than ever before.”
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