Terumo Medical Corporation950 Elkton Blvdelkton Md 21921 Pma Numberp140002 Supplement Numbers023 Date Received10 26 2022 Decision Date11 18 2022 Product Code Nip Advisory Committee Cardiovascular Supplement Type30 Day Notice Supplement Reason Process Change Manufacturer Sterilizer Packager Supplier Expedited Review Granted No

FDA Filings

This page includes the latest FDA filings for Terumo Medical Corporation950 Elkton Blvdelkton Md 21921 Pma Numberp140002 Supplement Numbers023 Date Received10 26 2022 Decision Date11 18 2022 Product Code Nip Advisory Committee Cardiovascular Supplement Type30 Day Notice Supplement Reason Process Change Manufacturer Sterilizer Packager Supplier Expedited Review Granted No. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Filings

Device Company	Device	Date
PMA P140002S023 TERUMO MEDICAL CORPORATION950 Elkton Blvdelkton, MD 21921 PMA NumberP140002 Supplement NumberS023 Date Received10/26/2022 Decision Date11/18/2022 Product Code NIP  Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	MISAGO® RX Self-expanding Peripheral Stent	2022-11-18