Aesculap L T D

FDA Filings

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

FDA Registration(s)

FDA Filings

Device Company	Device	Date
PMN K112671 AESCULAP, LTD.	STERILCONTAINER SYSTEM	2012-05-04

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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

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