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Nevro earns FDA clearance for SI joint fixation system

Nevro earned FDA 510(k) clearance to use its sacroiliac joint fixation system without having to include a lateral screw, the devicemaker said Feb. 28.

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Medtech news ASC leaders should know

Discover the latest developments in medtech, including FDA approvals, new appointments, and partnerships that ASC leaders should know about.

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Momentum Health earns FDA approval for AI spine app

Momentum Health earned FDA 510(k) clearance for Momentum Spine, an artificial intelligence-powered app for spine care.

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SI-Bone gets clearance for smaller version of spine implant

SI-Bone earned FDA 510(k) clearance of the iFuse Bedrock Granite implant system in a smaller diameter, according to a Jan. 30 news release.

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Curiteva gets FDA clearance for Inspire lumbar interbody system

Curiteva s Inspired 3D-printed lumbar interbody fusion system earned FDA 510(k) clearance, the devicemaker said Jan. 22.

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