documents: FDA-2023-N-2177-7035

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2023-N-2177-7035 FDA FDA-2023-N-2177 Reference 185 - FDA, “Modifications to Devices Subject to Premarket Approval (PMA)–The PMA Supplement Decision-Making Process; Guidance for Industry and FDA Staff,” December 11, 2008 Supporting & Related Material Background Material 2024-05-06T04:00:00Z 2024 5     2024-05-06T16:35:27Z   0 0 09000064865298ae

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