Glaukos Corporation229 Avenida Fabricantesan Clemente Ca 92672 Pma Numberp170043 Supplement Numbers014 Date Received05 31 2022 Decision Date08 29 2022 Product Code Ogo Advisory Committee Ophthalmic Supplement Typenormal 180 Day Track Supplement Reason Process Change Manufacturer Sterilizer Packager Supplier Expedited Review Granted No

FDA Filings

This page includes the latest FDA filings for Glaukos Corporation229 Avenida Fabricantesan Clemente Ca 92672 Pma Numberp170043 Supplement Numbers014 Date Received05 31 2022 Decision Date08 29 2022 Product Code Ogo Advisory Committee Ophthalmic Supplement Typenormal 180 Day Track 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 P170043S014 Glaukos Corporation229 Avenida Fabricantesan Clemente, CA 92672 PMA NumberP170043 Supplement NumberS014 Date Received05/31/2022 Decision Date08/29/2022 Product Code OGO  Advisory Committee Ophthalmic Supplement Typenormal 180 Day Track Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	iStent Trabecular Micro-Bypass Stent System, iStent inject Trabecular Micro-Bypass System, iStent inject W Trabecular Mi	2022-08-29