FDA 510(k) Applications Submitted by CryoLife, Inc.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K110581 |
03/01/2011 |
PROPATCH SOFT TISSUE REPAIR MATRIX |
CRYOLIFE, INC. |
| K101587 |
06/07/2010 |
PROPATCH SOFT TISSUE REPAIR MATRIX |
CRYOLIFE, INC. |
| K033484 |
11/04/2003 |
HUMAN HEART VALVE, CRYOVALVE SG |
CRYOLIFE, INC. |
| K172085 |
07/11/2017 |
PhotoFix Decellularized Bovine Pericardium |
CryoLife, Inc. |
| K162506 |
09/08/2016 |
PhotoFix Decellularized Bovine Pericardium |
CryoLife, Inc. |
| K183635 |
12/26/2018 |
PhotoFix Decellularized Bovine Pericardium |
CryoLife, Inc. |
| K091626 |
06/03/2009 |
CRYOPATCH SG PULMONARY HEMI-ARTERY; TRUNK; BRANCH |
CRYOLIFE, INC. |
| K101866 |
07/02/2010 |
CRYOPATCH SG PULMONARY HUMAN CARDIAC PATCH |
CRYOLIFE, INC. |
| K061892 |
07/03/2006 |
PROPATCH SOFT TISSUE REPAIR MATRIX |
CRYOLIFE, INC. |
| K092021 |
07/06/2009 |
CRYOVALVE SG PULMONARY HUMAN HEART VALVE (AND CONDUIT) |
CRYOLIFE, INC. |
| K083106 |
10/20/2008 |
CRYOVALVE SG PULMONARY VALVE AND CONDUIT |
CRYOLIFE, INC. |
| K132105 |
07/08/2013 |
PERCLOT TOPICAL |
CRYOLIFE, INC. |
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