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withdrawn,object_id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-N-2518-0003,FDA,FDA-2016-N-2518,Reference 1 - Authenticated U.S. Government Information GPO re Medical Devices; Custom Devices; Technical Amendment,Supporting & Related Material,Background Material,2016-10-13T04:00:00Z,2016,10,,,2016-10-13T15:57:02Z,,0,0,09000064822f4332
FDA-2016-N-2518-0004,FDA,FDA-2016-N-2518,Reference 2 - Guidance for Industry for Custom Device Exemption Final Guidance re Medical Devices; Custom Devices; Technical Amendment,Supporting & Related Material,Background Material,2016-10-13T04:00:00Z,2016,10,,,2016-10-13T15:57:14Z,,0,0,09000064822f4333
FDA-2016-N-2518-0002,FDA,FDA-2016-N-2518,List of References re Medical Devices; Custom Devices; Technical Amendment,Supporting & Related Material,Background Material,2016-10-13T04:00:00Z,2016,10,,,2016-10-13T15:56:45Z,,0,0,09000064822f4331
FDA-2016-N-2518-0001,FDA,FDA-2016-N-2518,Medical Devices: Custom Devices; Technical Amendment,Rule,Final Rule,2016-10-12T04:00:00Z,2016,10,2016-10-12T04:00:00Z,,2016-10-12T14:10:29Z,2016-24438,0,0,09000064822e6fe5