New titanium interbody for spinal fusions earns FDA clearance: 4 things to know

Innovasive received FDA 510(k) clearance for its DualX technology.

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Here are four things to know:

1. The titanium, dual expanding interbody device is designed for lumbar spinal fusion procedures.

2. Innovasive developed the technology using a family of titanium expandable interbody devices designed to be used in transforaminal lumbar interbody fusion, posterior lumbar interbody fusion and lateral lumbar interbody fusion procedures.

3. DualX’s portfolio features varying footprints, heights and lordosis degrees with post-expansion bone grafting.

4. Innovasive is a privately-held spinal device company that focuses on minimally invasive spine technologies.

More articles on surface technology:
1st cases of Life Spine’s expandable TLIF/PLIF spacer system performed: 3 observations
Porous PEEK superior to titanium-coated PEEK for osseointegration, study finds
UCSF invests in 3D-printed medical devices — 4 things to know

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