Atlas FDA

HUMAN HEART VALVE, CRYOVALVE SG

FDA 510(k) clearance K033484 · decided 2008-02-07

Clearance details

K-number
K033484
Device name
HUMAN HEART VALVE, CRYOVALVE SG
Applicant
Cryolife, Inc.
Decision
Substantially Equivalent
Date received
2003-11-04
Decision date
2008-02-07
Days to decision
1556 days
Clearance type
Traditional
Product code
OHA
Device class
U
Medical specialty
Unknown
Advisory committee
Unknown
Location
Kennesaw, GA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
CryoValve SG Pulmonary Valve (SGPV10) CryoValve SG Pulmonary Valve and Conduit (SGPV00) (K252059)Artivion, Inc.2025-10-02
CRYOVALVE SG PULMONARY HUMAN HEART VALVE (AND CONDUIT) (K092021)Cryolife, Inc.2010-05-25
CRYOVALVE SG PULMONARY VALVE AND CONDUIT (K083106)Cryolife, Inc.2009-02-06

Recalls involving this device

RecordFirmDate
CryoValve, Aortic Valve & Conduit recall (Z-1523-2008)CryoLife, Inc.2008-09-01
CryoValve, Pulmonary Valve & Conduit recall (Z-1524-2008)CryoLife, Inc.2008-09-01

PMA approvals by this applicant

RecordFirmDate
BioGlue® Surgical Adhesive (P010003/S042)Cryolife, Inc.2025-03-18
BioGlue® Surgical Adhesive (P010003/S041)Cryolife, Inc.2023-10-20
CardioGenesis TMR System (P970029/S040)Cryolife, Inc.2022-09-01
BioGlue Surgical Adhesive (P010003/S040)Cryolife, Inc.2022-05-25
BioGlue® Surgical Adhesive (P010003/S039)Cryolife, Inc.2021-12-09
BioGlue Surgical Adhesive (P010003/S038)Cryolife, Inc.2021-07-23
TMR Holmium Laser System (P970029/S038)Cryolife, Inc.2021-01-21
BioGlue Surgical Adhesive (P010003/S037)Cryolife, Inc.2019-12-20