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withdrawn,object_id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-2012-N-1239-0004,FDA,FDA-2012-N-1239,"Dental Devices; Reclassification of Temporary Mandibular Condyle
Prosthesis",Rule,Final Rule,2013-12-30T05:00:00Z,2013,12,2013-12-30T05:00:00Z,,2013-12-30T15:21:52Z,2013-31217,0,0,09000064814e1b8c
FDA-2012-N-1239-0002,FDA,FDA-2012-N-1239,Draft Guideline for Industry and Food and Drug Administration Staff; Class II Special Controls Guideline: Temporary Mandibular Condyle Reconstruction Plate,Other,Guidance,2013-02-07T05:00:00Z,2013,2,2013-02-07T05:00:00Z,,2024-11-07T22:48:58Z,,1,0,09000064811e9c9d
FDA-2012-N-1239-0001,FDA,FDA-2012-N-1239,Dental Devices: Reclassification of Temporary Mandibular Condyle Prosthesis,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-02-07T05:00:00Z,2013,2,2013-02-07T05:00:00Z,2013-05-09T03:59:59Z,2014-01-14T13:06:51Z,2013-02688,0,0,09000064811ea30e