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withdrawn,object_id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-2021-N-0855-0001,FDA,FDA-2021-N-0855,"Medical Devices; Neurological
Devices; Classification of the
Cerebrospinal Fluid Shunt System",Rule,Final Rule,2021-12-29T05:00:00Z,2021,12,2021-12-29T05:00:00Z,,2021-12-29T17:26:25Z,2021-28157,0,0,0900006484effaf3