Stryker (SYK) announced that its OptaBlate basivertebral nerve ablation system received 510(k) clearance from the Food and Drug Administration. OptaBlate BVNA is used in a targeted minimally invasive procedure providing vertebrogenic pain relief, the company said in a statement. “The addition of the OptaBlate BVN to Stryker’s pain portfolio expands its advanced pain therapy solutions for patients and is an intersection of its two core competencies: radiofrequency ablation technology and vertebral access,” it added.
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