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withdrawn,object_id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-2017-N-6730-0041,FDA,FDA-2017-N-6730,Medical Devices and Device-Led Combination Products; Voluntary Malfunction Summary Reporting for Manufacturers,Rule,Final Rule,2024-08-29T04:00:00Z,2024,8,,,2024-08-29T13:19:24Z,2024-19414,0,0,09000064866b35bb