The aprevo® Personalized Spine Procedure is the only intervertebral spine implant that is personalized for you.

The FDA Breakthrough Device Designation

Unique. Innovative. Breakthrough.

aprevo® is the first intervertebral spine implant to receive FDA Breakthrough Device designation as well as the Transformative New Technology designation from the Centers for Medicare & Medicaid Services (CMS).

Furthermore, aprevo® is the first spine technology breakthrough device to obtain marketing authorization from the FDA.1

We are all different and unique. Your spine implant should be, too.

It all begins with YOU.

Talk to your doctor about the aprevo® patient-specific spinal implants, or find a doctor with our surgeon locator.

Find a Provider

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References:

  1. Breakthrough Device Designation. U.S. Food and Drug Administration. November, 2023