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withdrawn,object_id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-2015-M-2739-0002,FDA,FDA-2015-M-2739,Medical Devices: Availability of Safety and Effectiveness Summaries for Premarket Approval Applications,Notice,Notice of Approval,2015-11-18T05:00:00Z,2015,11,2015-11-18T05:00:00Z,,2024-11-07T23:34:52Z,2015-29450,1,0,0900006481d56bc9
FDA-2015-M-2739-0001,FDA,FDA-2015-M-2739,"Premarket Approval Response from FDA CDRH to Minerva Surgical, Inc.
Minerva Endometrial Ablation Device",Other,Approval,2015-09-16T04:00:00Z,2015,9,2015-09-16T04:00:00Z,,2015-09-16T17:24:42Z,,0,0,0900006481c79e42