Aesculap Implant Systems

FDA Filings

This page includes the latest FDA filings for Aesculap Implant Systems. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Owner/Operator Registration

FDA Filings

Device Company	Device	Date
PMN K140452 AESCULAP IMPLANT SYSTEMS	VEGA KNEE SYSTEM	2014-03-25
PMN K121879 AESCULAP IMPLANT SYSTEMS	VEGA KNEE SYSTEM	2012-07-27
PMN K101815 AESCULAP IMPLANT SYSTEMS	ENDURO KNEE SYSTEM	2010-12-20
PMN K100623 AESCULAP IMPLANT SYSTEMS	AESCULAP IMPLANT SYSTEMS S4 SPINAL SYSTEM	2010-06-09
PMN K090299 AESCULAP IMPLANT SYSTEMS	BIOLOX OPTION CERAMIC FEMORAL HEAD AND METHA XL HEADS	2009-04-24
PMN K071945 AESCULAP IMPLANT SYSTEMS	S4 SPINAL SYSTEM	2007-09-20

Similar & Related FDA Registered Companies

• Aesculap Inc. / Aesculap Implant Systems, LLC
• AESCULAP IMPLANT SYSTEMS, LLC
• Aesculap Implants Systems, LLC
• Aesculap Implants Systems, Inc.
• Aesculap Implant Systems, Inc.
• 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