# Guidance Document for the Preparation of IDEs for Spinal Systems - Guidance for Industry and/or FDA Staff - FDA Guidance Document Source: https://www.globalkeysolutions.net/guidances/guidance-document/guidance-document-for-the-preparation-of-ides-for-spinal-systems-guidance-for-industry-andor-fda-staff/53834649-62f5-4529-8bab-38ce98dfca81 > FDA guidance document: Guidance Document for the Preparation of IDEs for Spinal Systems - Guidance for Industry and/or FDA Staff. Issue date: January 12, 2000. Get complete insights and analysis. --- ## Details - Title: Guidance Document for the Preparation of IDEs for Spinal Systems - Guidance for Industry and/or 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: 2000-01-12 - Last Changed: 2024-04-11 - Docket Number: FDA-2020-D-0957 ## Related Documents - [Guidance on 510(k) Submissions for Keratoprostheses - Guidance for Industry and for FDA Reviewers/Staff](https://www.globalkeysolutions.net/guidances/guidance-document/guidance-on-510k-submissions-for-keratoprostheses-guidance-for-industry-and-for-fda-reviewersstaff/f9cc0274-42dd-4e68-9f13-368ab5523dd3) - [Aqueous Shunts - 510(k) Submissions - Guidance for Industry and for FDA Reviewers/Staff](https://www.globalkeysolutions.net/guidances/guidance-document/aqueous-shunts-510k-submissions-guidance-for-industry-and-for-fda-reviewersstaff/17f37714-5103-4981-9daf-822fd5d810e3) - [Guidance for the Preparation of a Premarket Notification Application for a Surgical Mesh - Guidance for Industry and/or for FDA Reviewers/Staff and/or Compliance](https://www.globalkeysolutions.net/guidances/guidance-document/guidance-for-the-preparation-of-a-premarket-notification-application-for-a-surgical-mesh-guidance-for-industry-andor-for-fda-reviewersstaff-andor-compliance/a7ca09bf-4f01-43f3-b44b-7f175a8feb84)