Smith Nephew Inc 1450 Brooks Roadmemphis Tn 38116 Pma Numberp150030 Supplement Numbers023 Date Received07 14 2022 Decision Date08 08 2022 Product Code Mra 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 Smith Nephew Inc 1450 Brooks Roadmemphis Tn 38116 Pma Numberp150030 Supplement Numbers023 Date Received07 14 2022 Decision Date08 08 2022 Product Code Mra 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 Registration(s)

FDA Filings

Device
Company
DeviceDate
Smith & Nephew, Inc.1450 Brooks Roadmemphis, TN 38116 PMA NumberP150030 Supplement NumberS023 Date Received07/14/2022 Decision Date08/08/2022 Product Code MRA  Advisory Committee Orthopedic Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
R3TM Delta Ceramic Acetabular System2022-08-08

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