id,agency_id,docket_id,title,document_type,subtype,posted_date,posted_year,posted_month,comment_start_date,comment_end_date,last_modified,fr_doc_num,open_for_comment,withdrawn,object_id
FDA-2016-D-1159-0007,FDA,FDA-2016-D-1159,"FDA Categorization of Investigational Device Exemption (IDE) Devices to Assist the Centers for Medicare and Medicaid Services (CMS) with  Coverage Decisions Guidance for Sponsors, Clinical Investigators, Industry, Institutional Review Boards, and Food and Drug Administration Staff",Other,Guidance,2017-12-05T05:00:00Z,2017,12,2017-12-05T05:00:00Z,,2024-11-07T01:12:06Z,,1,0,0900006482ce1245
FDA-2016-D-1159-0006,FDA,FDA-2016-D-1159,"Food and Drug Administration Categorization of Investigational Device Exemption Devices To Assist the Centers for Medicare and Medicaid
Services With Coverage Decisions; Guidance for Sponsors, Clinical
Investigators, Industry, Institutional Review Boards, and Food and Drug
Administration Staff; Availability",Notice,Notice of Availability,2017-12-05T05:00:00Z,2017,12,2017-12-05T05:00:00Z,,2017-12-05T17:07:32Z,2017-26195,0,0,0900006482cdbd97