Fidia Farmaceutici S P A Via Ponte Della Fabbrica 3 Aabano Terme 35031 Pma Numberp180040 Supplement Numbers002 Date Received07 11 2022 Decision Date08 08 2022 Product Code Moz Advisory Committee Orthopedic 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 Fidia Farmaceutici S P A Via Ponte Della Fabbrica 3 Aabano Terme 35031 Pma Numberp180040 Supplement Numbers002 Date Received07 11 2022 Decision Date08 08 2022 Product Code Moz Advisory Committee Orthopedic 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 P180040S002 Fidia Farmaceutici S.p.A.via Ponte Della Fabbrica 3/aabano Terme 35031 PMA NumberP180040 Supplement NumberS002 Date Received07/11/2022 Decision Date08/08/2022 Product Code MOZ  Advisory Committee Orthopedic Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	TRILURON®	2022-08-08