Cryolife Inc 1655 Roberts Blvd N W Kennesaw Ga 30144 Pma Numberp010003 Supplement Numbers040 Date Received04 29 2022 Decision Date05 25 2022 Product Code Muq Advisory Committee Cardiovascular 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 Cryolife Inc 1655 Roberts Blvd N W Kennesaw Ga 30144 Pma Numberp010003 Supplement Numbers040 Date Received04 29 2022 Decision Date05 25 2022 Product Code Muq Advisory Committee Cardiovascular 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
CRYOLIFE, INC.1655 Roberts Blvd., N.w.kennesaw, GA 30144 PMA NumberP010003 Supplement NumberS040 Date Received04/29/2022 Decision Date05/25/2022 Product Code MUQ  Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
BioGlue Surgical Adhesive2022-05-25

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