documents: FDA-2017-M-6984-0001

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-M-6984-0001 FDA FDA-2017-M-6984 Premarket Approval Response from FDA CDRH to Medtronic, Inc. Implantable System for Remodulin Other Letter(s) 2018-02-05T05:00:00Z 2018 2 2018-02-05T05:00:00Z   2018-02-05T14:37:37Z   0 0 0900006482eeaa8b

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