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www.fdanews.com/articles/198239-fda-clears-stratus-cannula-for-radiofrequency-heat-lesion-procedures

FDA Clears Stratus’ Cannula for Radiofrequency Heat-Lesion Procedures

July 28, 2020

Utah-based Stratus Medical has received 510(k) clearance from the FDA for its Vesta RF cannula for radiofrequency heat-lesion procedures for relieving pain.

The Vesta RF is for use in clinical situations where the Nimbus, the company’s large-volume heat-lesion device, is not usable.

The device earned a CE mark in 2018 and has been used in thousands of procedures in Australia and Brazil.

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