Aesculap Implant Systems Llc3773 Corporate Parkwaycenter Valley Pa 18034 Pma Numberp120024 Supplement Numbers012 Date Received06 13 2022 Decision Date06 24 2022 Product Code Mjo 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 Aesculap Implant Systems Llc3773 Corporate Parkwaycenter Valley Pa 18034 Pma Numberp120024 Supplement Numbers012 Date Received06 13 2022 Decision Date06 24 2022 Product Code Mjo 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 Filings

Device Company	Device	Date
PMA P120024S012 AESCULAP IMPLANT SYSTEMS, LLC3773 Corporate Parkwaycenter Valley, PA 18034 PMA NumberP120024 Supplement NumberS012 Date Received06/13/2022 Decision Date06/24/2022 Product Code MJO  Advisory Committee Orthopedic Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	activL Artificial Disc	2022-06-24