# Preparation and Review of Investigational Device Exemption Applications (IDEs) for Total Artificial Discs: Guidance for Industry and FDA Staff - FDA Guidance Document Source: https://www.globalkeysolutions.net/guidances/guidance-document/preparation-and-review-of-investigational-device-exemption-applications-ides-for-total-artificial-discs-guidance-for-industry-and-fda-staff/c0f2683e-9f2f-4a30-9074-61d1242a7e6f > FDA guidance document: Preparation and Review of Investigational Device Exemption Applications (IDEs) for Total Artificial Discs: Guidance for Industry and FDA Staff. Issue date: April 11, 2008. Get complete insights and analysis. --- ## Details - Title: Preparation and Review of Investigational Device Exemption Applications (IDEs) for Total Artificial Discs: Guidance for Industry and FDA Staff - Communication Type: Guidance Document - Product Type: devices - Office Name: Center for Devices and Radiological Health - Office URL: /offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7 - Issue Date: 2008-04-11 - Last Changed: 2020-03-20 - Docket Number: FDA-2020-D-0957 ## Related Documents - [Clinical Data Presentations for Orthopedic Device Applications - Guidance for Industry and FDA Staff](https://www.globalkeysolutions.net/guidances/guidance-document/clinical-data-presentations-for-orthopedic-device-applications-guidance-for-industry-and-fda-staff/b5acd4ee-cac5-446d-9a45-76683dae10e5) - [Guidance for Industry and FDA Staff: Spinal System 510(k)s](https://www.globalkeysolutions.net/guidances/guidance-document/guidance-for-industry-and-fda-staff-spinal-system-510ks/7741b13b-29da-41e1-bdad-60df446c7b43) - [Hemodialysis Blood Tubing Sets - Premarket Notification [510(k)] Submissions: Guidance for Industry and FDA Staff](https://www.globalkeysolutions.net/guidances/guidance-document/hemodialysis-blood-tubing-sets-premarket-notification-510k-submissions-guidance-for-industry-and-fda-staff/a50fef58-09c4-45a9-95b7-61eff98924c0)