DiFusion receives FDA clearance for spinal interbody device — 4 insights

The FDA granted DiFusion 510(k) clearance for its Xiphos-Zfuze spinal interbody device.

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Four insights:

1. Xiphos-ZF is the first implant developed from a new biomaterial called Zfuze.

2. Zfuze is a load-bearing biomaterial that evokes a pro-reparative macrophage phenotype rather than a pro-inflammatory phenotype.

3. Paul Kraemer, MD, of Indiana Spine Group in Carmel is set to perform the first spinal surgery with Xiphos-ZF.

4. DiFusion will launch Xiphos-ZF in the fourth quarter.

More articles on devices:
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Price transparency, value-based care & bundles: Altair Health CEO aims to drive change in spine
Stryker receives FDA clearance for 3D-printed expandable interbody device — 4 things to know

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