Ferrosan Meidcal Devices A Ssydmarken 5soeborg 08876 Pma Numberp990004 Supplement Numbers055 Date Received06 27 2022 Decision Date12 21 2022 Product Code Lmf Advisory Committee General Plastic Surgery Supplement Type135 Review Track For 30 Day Notice Supplement Reason Process Change Manufacturer Sterilizer Packager Supplier Expedited Review Granted No

FDA Filings

This page includes the latest FDA filings for Ferrosan Meidcal Devices A Ssydmarken 5soeborg 08876 Pma Numberp990004 Supplement Numbers055 Date Received06 27 2022 Decision Date12 21 2022 Product Code Lmf Advisory Committee General Plastic Surgery Supplement Type135 Review Track For 30 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
Ferrosan Meidcal Devices A/Ssydmarken 5soeborg 08876 PMA NumberP990004 Supplement NumberS055 Date Received06/27/2022 Decision Date12/21/2022 Product Code LMF  Advisory Committee General & Plastic Surgery Supplement Type135 Review Track For 30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
SURGIFOAM Absorabable Gelatin Sponge, U.S.P., SURGIFLO Hemostatic Matrix, SURGIFLO Hemostatic MatrixKit with Thrombin2022-12-21

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