Merz North America Inc4133 Courtney Roadsuite 10franksville Wi 53126 Pma Numberp040047 Supplement Numbers069 Date Received12 15 2022 Decision Date01 12 2023 Product Code Lnm Advisory Committee Gastroenterology Urology 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 Merz North America Inc4133 Courtney Roadsuite 10franksville Wi 53126 Pma Numberp040047 Supplement Numbers069 Date Received12 15 2022 Decision Date01 12 2023 Product Code Lnm Advisory Committee Gastroenterology Urology 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 P040047S069 MERZ NORTH AMERICA, INC4133 Courtney Roadsuite 10franksville, WI 53126 PMA NumberP040047 Supplement NumberS069 Date Received12/15/2022 Decision Date01/12/2023 Product Code LNM  Advisory Committee Gastroenterology/Urology Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	P040047 COAPTITE® Injectable Implant	2023-01-12