Stryker Says OptaBlate Receives FDA Clearance for Low Back Pain Relief

MT Newswires Live
20 May

Stryker (SYK) said Monday its OptaBlate basivertebral nerve ablation system received 510(k) clearance from the US Food and Drug Administration.

OptaBlate is used in a minimally invasive procedure to provide relief from vertebrogenic low back pain, the company said.

Stryker said the system, which expands its advanced pain therapy portfolio, combines its competencies in radiofrequency ablation and vertebral access.

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