Depuy Inc P O Box 988700 Orthopaedic Drivewarsaw In 46581 0988 Pma Numberp830055 Supplement Numbers303 Date Received01 11 2023 Decision Date02 01 2023 Product Code Njl 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 Depuy Inc P O Box 988700 Orthopaedic Drivewarsaw In 46581 0988 Pma Numberp830055 Supplement Numbers303 Date Received01 11 2023 Decision Date02 01 2023 Product Code Njl 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 Registration(s)

FDA Filings

Device
Company
DeviceDate
DEPUY, INC.p.o. Box 988700 Orthopaedic Drivewarsaw, IN 46581-0988 PMA NumberP830055 Supplement NumberS303 Date Received01/11/2023 Decision Date02/01/2023 Product Code NJL  Advisory Committee Orthopedic Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
LCS® Total Knee System2023-02-01

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