Johnson Johnson Surgical Vision Inc 31 Technology Drivesuite 200irvine Ca 92618 Pma Numberp080010 Supplement Numbers021 Date Received11 09 2022 Decision Date12 06 2022 Product Code Mfk Advisory Committee Ophthalmic 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 Johnson Johnson Surgical Vision Inc 31 Technology Drivesuite 200irvine Ca 92618 Pma Numberp080010 Supplement Numbers021 Date Received11 09 2022 Decision Date12 06 2022 Product Code Mfk Advisory Committee Ophthalmic 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 P080010S021 Johnson & Johnson Surgical Vision, Inc.31 Technology Drivesuite 200irvine, CA 92618 PMA NumberP080010 Supplement NumberS021 Date Received11/09/2022 Decision Date12/06/2022 Product Code MFK  Advisory Committee Ophthalmic Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	TECNIS® Multifocal Foldable Posterior Chamber IOL	2022-12-06