Merz North America Inc4133 Courtney Roadsuite 10franksville Wi 53126 Pma Numberp040047 Supplement Numbers066 Date Received11 01 2022 Decision Date11 22 2022 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 Numbers066 Date Received11 01 2022 Decision Date11 22 2022 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 P040047S066 MERZ NORTH AMERICA, INC4133 Courtney Roadsuite 10franksville, WI 53126 PMA NumberP040047 Supplement NumberS066 Date Received11/01/2022 Decision Date11/22/2022 Product Code LNM  Advisory Committee Gastroenterology/Urology Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	COAPTITE® Injectable Implant	2022-11-22