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13
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15 devices found
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Manufacturer: Cryolife, Inc.
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Class
PhotoFix Decellularized Bovine Pericardium
Cryolife, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K183635
Active
Cleared 14 Feb 2019
Active
510(k)
510(k)
II
3 variants
PhotoFix Decellularized Bovine Pericardium
K162506
PhotoFix Decellularized Bovine Pericardium
K172085
Cryovalve Sg Pulmonary Human Heart Valve (And Conduit)
Open recall
Cryolife, Inc.
·
,
United States
(FDA 510(k) applicant)
Unclassified
FDA 510(k)
K092021
Active
Cleared 25 May 2010
Active
510(k)
510(k)
—
Cryopatch Sg Pulmonary Hemi-Artery; Trunk; Branch
Open recall
Cryolife, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K091626
Active
Cleared 7 Aug 2009
Active
510(k)
510(k)
II
Perclot Topical
Cryolife, Inc.
·
,
United States
(FDA 510(k) applicant)
Unclassified
FDA 510(k)
K132105
Active
Cleared 3 Apr 2014
Active
510(k)
510(k)
—
Cryopatch Sg Pulmonary Human Cardiac Patch
Cryolife, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K101866
Active
Cleared 23 Jul 2010
Active
510(k)
510(k)
II
Propatch Soft Tissue Repair Matrix
Cryolife, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K061892
Active
Cleared 22 Nov 2006
Active
510(k)
510(k)
II
3 variants
Propatch Soft Tissue Repair Matrix
K101587
Propatch Soft Tissue Repair Matrix
K110581
Human Heart Valve, Cryovalve Sg
Cryolife, Inc.
·
,
United States
(FDA 510(k) applicant)
Unclassified
FDA 510(k)
K033484
Active
Cleared 7 Feb 2008
Active
510(k)
510(k)
—
Cryovalve Sg Pulmonary Valve And Conduit
Cryolife, Inc.
·
,
United States
(FDA 510(k) applicant)
Unclassified
FDA 510(k)
K083106
Active
Cleared 6 Feb 2009
Active
510(k)
510(k)
—
Hero Graft
Hemoshpere, Inc., A Cryolife Company
·
,
FDA registration: United States
Class II
FDA 510(k)
K124039
Active
Cleared 7 Mar 2013
Active
510(k)
510(k)
II
Eclipse Tmr Holmium Laser System
Cryolife, Inc.
·
,
United States
(FDA 510(k) applicant)
Class III
FDA PMA
P970029
Active
Approved 11 Feb 1999
Active
PMA
PMA
III
Bioglue Surgical Adhesive
Cryolife, Inc.
·
,
United States
(FDA 510(k) applicant)
Class III
FDA PMA
P010003
Active
Approved 3 Dec 2001
Active
PMA
PMA
III
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