Biomet Manufacturing Corp 56 East Bell Drivep O Box 587warsaw In 46581 0587 Pma Numberp010014 Supplement Numbers103 Date Received09 29 2022 Decision Date10 25 2022 Product Code Nra 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 Biomet Manufacturing Corp 56 East Bell Drivep O Box 587warsaw In 46581 0587 Pma Numberp010014 Supplement Numbers103 Date Received09 29 2022 Decision Date10 25 2022 Product Code Nra 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 P010014S103 BIOMET MANUFACTURING CORP.56 East Bell Drivep.o. Box 587warsaw, IN 46581-0587 PMA NumberP010014 Supplement NumberS103 Date Received09/29/2022 Decision Date10/25/2022 Product Code NRA  Advisory Committee Orthopedic Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	Oxford® Partial Knee System	2022-10-25