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Technical Considerations for Additive Manufactured Medical Devices: Guidance for Industry and Food and Drug Administration Staff
Technical Considerations for Additive Manufactured Medical Devices: Guidance for Industry and Food and Drug Administration Staff
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FDA 官方历史目录记录；Final guidance；发布日期：2017-12-05。官方主题：Premarket, Biotechnology, 510(k), Premarket Approval (PMA), Investigational Device Exemption (IDE), HUD/HDE, Orthopedic, Tissue。请通过官方原文与附件查阅文件。
来源：FDA Guidance Documents · fda.gov