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withdrawn,object_id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-2013-N-1529-0020,FDA,FDA-2013-N-1529,"Medical Device Classification Procedures: Incorporating Food and
Drug Administration Safety and Innovation Act Procedures",Rule,Final Rule,2018-12-17T05:00:00Z,2018,12,2018-12-17T05:00:00Z,,2018-12-17T14:46:15Z,2018-27015,0,0,090000648399cf84