Depuy A Johnson Johnson Co

FDA Filings

This page includes the latest FDA filings for Depuy A Johnson Johnson Co. 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
PMA P960054 DEPUY, A JOHNSON & JOHNSON CO.	S-ROM POLY-DIAL CONSTRAINED LINER	1997-06-19

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• DEPUY, A JOHNSON & JOHNSON CO.p.o. Box 988700 Orthopaedic Drivewarsaw, IN 46581-0988 PMA NumberP960054 Supplement NumberS003 Date Received08/10/1999 Decision Date12/22/1999 Reclassified Date 05/30/2002 Product Code KWZ  Advisory Committee Orthopedic Supplement Typenormal 180 Day Track Supplement Reason Location Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
• DEPUY, A JOHNSON & JOHNSON CO.p.o. Box 988700 Orthopaedic Drivewarsaw, IN 46581-0988 PMA NumberP960054 Supplement NumberS002 Date Received07/30/1999 Decision Date12/07/1999 Reclassified Date 05/30/2002 Product Code KWZ  Advisory Committee Orthopedic Supplement Typenormal 180 Day Track Supplement Reason Change Design/components/specifications/material Expedited Review Granted? No
• DEPUY, A JOHNSON & JOHNSON CO.p.o. Box 988700 Orthopaedic Drivewarsaw, IN 46581-0988 PMA NumberP960054 Supplement NumberS004 Date Received10/06/1999 Decision Date11/10/1999 Reclassified Date 05/30/2002 Product Code KWZ  Advisory Committee Orthopedic Supplement Typenormal 180 Day Track Supplement Reason Location Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No