Cryolife, Inc. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
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.
FDA 510(k) cleared devices by Cryolife, Inc.
12 devices
Cleared
Feb 14, 2019
PhotoFix Decellularized Bovine Pericardium
Cardiovascular
50d
Cleared
Dec 04, 2017
PhotoFix Decellularized Bovine Pericardium
Cardiovascular
146d
Cleared
Mar 09, 2017
PhotoFix Decellularized Bovine Pericardium
Cardiovascular
182d
Cleared
Apr 03, 2014
PERCLOT TOPICAL
General & Plastic Surgery
269d
Cleared
Jan 10, 2012
PROPATCH SOFT TISSUE REPAIR MATRIX
General & Plastic Surgery
315d
Cleared
Sep 16, 2010
PROPATCH SOFT TISSUE REPAIR MATRIX
General & Plastic Surgery
101d
Cleared
Jul 23, 2010
CRYOPATCH SG PULMONARY HUMAN CARDIAC PATCH
Cardiovascular
21d
Cleared
May 25, 2010
CRYOVALVE SG PULMONARY HUMAN HEART VALVE (AND CONDUIT)
Cardiovascular
323d
Cleared
Aug 07, 2009
CRYOPATCH SG PULMONARY HEMI-ARTERY
Cardiovascular
65d
Cleared
Feb 06, 2009
CRYOVALVE SG PULMONARY VALVE AND CONDUIT
Cardiovascular
109d
Cleared
Feb 07, 2008
HUMAN HEART VALVE, CRYOVALVE SG
Cardiovascular
1556d
Cleared
Nov 22, 2006
PROPATCH SOFT TISSUE REPAIR MATRIX
General & Plastic Surgery
142d