Stryker Gets FDA 510(k) Clearance for OptaBlate System

Dow Jones

05/20

By Chris Wack

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

The medical technology company said its OptaBlate BVNA is used in a targeted minimally invasive procedure providing long-lasting vertebrogenic pain relief.

Stryker said the OptaBlate system achieves at least a 1-centimeter lesion in seven minutes, and its microinfusion technology, which keeps the zone hydrated, reduces impedance errors and prevents charring.

Write to Chris Wack at chris.wack@wsj.com

(END) Dow Jones Newswires

May 19, 2025 13:19 ET (17:19 GMT)

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