Atlas FDA

PhotoFix Decellularized Bovine Pericardium

FDA 510(k) clearance K183635 · decided 2019-02-14

Clearance details

K-number
K183635
Device name
PhotoFix Decellularized Bovine Pericardium
Applicant
Cryolife, Inc.
Decision
Substantially Equivalent
Date received
2018-12-26
Decision date
2019-02-14
Days to decision
50 days
Clearance type
Special
Product code
PSQ
Device class
2
Regulation number
870.3470
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
Kennesaw, GA, US
Third-party review
No
Expedited review
No

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CorMatrix Cor Patch (3 cm x 5 cm)(single pack), CorMatrix Cor Patch (4 cm x 7 cm)(single pack), CorMatrix Cor Patch (7 cm x 10 cm)(single pack) (K181038)Cormatrix Cardiovascular, Inc.2018-10-10
PhotoFix Decellularized Bovine Pericardium (K172085)Cryolife, Inc.2017-12-04
Duravess bovine pericardial vascular patch (K172660)Edwards Lifesciences, LLC2017-11-17
CardioCel 3D (K170951)Admedus Regen Pty, Ltd.2017-04-28

Recalls involving this device

No recalls on record reference this clearance.

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