Viseon earns FDA clearance for minimally invasive spine surgery system: 5 highlights

Viseon received FDA 510(k) clearance for its Voyant System for minimally invasive spine surgery.

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Here are five highlights:

1. The system features proprietary HD imaging sensors and illumination technology.

2. Viseon designed the system as a sterile single-use, disposable retractor device with integrated visualization technology.

3. Additionally, the Voyant System includes a reusable controller that enables digital, intraoperative manipulation of the surgical site image.

4. According to Viseon President and CEO Jeffrey Valko, spine surgeons have been slow to adopt minimally invasive spine surgery because of the inconsistent outcomes due to lack of direct access and visibility.

5. Viseon’s platform technology has been used in posterior lumbar decompression and interbody fusion procedures. Currently, the company is expanding the platform to include lumbar lateral access and anterior cervical decompression fusion applications.

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