Cochlear Americas13059 East Peakview Avenuecentennial Co 80111 Pma Numberp130016 Supplement Numbers050 Date Received07 11 2022 Advisory Committee Ear Nose Throat 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 Cochlear Americas13059 East Peakview Avenuecentennial Co 80111 Pma Numberp130016 Supplement Numbers050 Date Received07 11 2022 Advisory Committee Ear Nose Throat 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 P130016S050 Cochlear Americas13059 East Peakview Avenuecentennial, CO 80111 PMA NumberP130016 Supplement NumberS050 Date Received07/11/2022 Advisory Committee Ear Nose & Throat Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	Nucleus® Hybrid™ L24 Cochlear Implant System	1969-12-31