Medtronic Sofamor Danek Usa

FDA Filings

This page includes the latest FDA filings for Medtronic Sofamor Danek Usa. 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
PMN K214010 Medtronic Sofamor Danek USA	Anteralign Spinal System With Titan NanoLOCK Surface Technology	2022-04-12
PMN K170347 Medtronic Sofamor Danek USA	CD HORIZON™ Fenestrated Screw Set	2017-04-04
PMN K133904 MEDTRONIC SOFAMOR DANEK USA	CD HORIZON SPINAL SYSTEM GROWTH ROD SET	2014-02-25

Similar & Related FDA Registered Companies

• MEDTRONIC SOFAMOR DANEK USA, INC
• Medtronic Sofamor Danek USA, Inc.1800 Pyramid Placememphis, TN 38132 PMA NumberP000058 Supplement NumberS087 Date Received07/21/2022 Decision Date08/09/2022 Product Code NEK  Advisory Committee Orthopedic Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
• Medtronic Sofamor Danek USA, Inc.1800 Pyramid Placememphis, TN 38132 PMA NumberP000054 Supplement NumberS068 Date Received07/21/2022 Decision Date08/09/2022 Product Code MPW  Advisory Committee Orthopedic Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
• Medtronic Sofamor Danek USA, Inc.1800 Pyramid Placememphis, TN 38132 PMA NumberP000054 Supplement NumberS067 Date Received05/10/2022 Decision Date06/09/2022 Product Code MPW  Advisory Committee Orthopedic Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
• Medtronic Sofamor Danek USA, Inc.1800 Pyramid Placememphis, TN 38132 PMA NumberP000058 Supplement NumberS086 Date Received05/10/2022 Decision Date06/08/2022 Product Code NEK  Advisory Committee Orthopedic Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No