# FDA Grants PMA to Artivion AMDS Hybrid Prosthesis for Acute Aortic Dissection

> fda · REPORTED · 2026-06-01

The FDA granted Premarket Approval to Artivion's AMDS Hybrid Prosthesis, a device for treating acute DeBakey Type I aortic dissections, marking a significant regulatory milestone for this cardiovascular device.

- Company: Artivion
- Sector: medical devices
- Primary source: https://www.rttnews.com/content/biotechnology.aspx

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Source: MedFuel Intel news monitor. Verification tier: REPORTED. Informational only, not investment advice. Corrections: media@medfuelinc.com.