Zimmer Inc P O Box 708warsaw In 46581 0708 Pma Numberp060037 Supplement Numbers082 Date Received09 30 2022 Decision Date10 06 2022 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 Zimmer Inc P O Box 708warsaw In 46581 0708 Pma Numberp060037 Supplement Numbers082 Date Received09 30 2022 Decision Date10 06 2022 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
ZIMMER, INC.p.o. Box 708warsaw, IN 46581-0708 PMA NumberP060037 Supplement NumberS082 Date Received09/30/2022 Decision Date10/06/2022 Product Code NJL  Advisory Committee Orthopedic Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
NexGen® LPS-Flex/LPS Mobile Bearing Knee System2022-10-06

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