Cryolife, Inc. - FDA 510(k) Cleared Devices

Cryolife, Inc. has 12 FDA 510(k) cleared medical devices. Based in Kennesaw, US.

Historical record: 12 cleared submissions from 2006 to 2019. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Cryolife, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Artivion, Inc. as regulatory consultant.