Atlas FDA

BIOGLUE

FDA premarket approval P010003/S012 · decided 2008-06-24

Approval details

PMA number
P010003
Supplement
S012
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
BIOGLUE
Generic name
Glue, surgical, arteries
Applicant
Cryolife, Inc.
Date received
2008-06-06
Decision date
2008-06-24
Days to decision
18 days
Decision code
OK30
Product code
MUQ
Advisory committee
Cardiovascular
Expedited review
No
Location
Kennesaw, GA
Statement
ADDITION OF AN AUTOMATED PUMP FOR DISPENSING BOVINE SERUM ALBUMIN AND GLUTERALDEHYDE IN THE MANUFACTURE OF BIOGLUE® SURGICAL ADHESIVE.

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510(k) clearances by this applicant

RecordFirmDate
PhotoFix Decellularized Bovine Pericardium (K183635)Cryolife, Inc.2019-02-14
PhotoFix Decellularized Bovine Pericardium (K172085)Cryolife, Inc.2017-12-04
PhotoFix Decellularized Bovine Pericardium (K162506)Cryolife, Inc.2017-03-09
PERCLOT TOPICAL (K132105)Cryolife, Inc.2014-04-03
PROPATCH SOFT TISSUE REPAIR MATRIX (K110581)Cryolife, Inc.2012-01-10
PROPATCH SOFT TISSUE REPAIR MATRIX (K101587)Cryolife, Inc.2010-09-16
CRYOPATCH SG PULMONARY HUMAN CARDIAC PATCH (K101866)Cryolife, Inc.2010-07-23
CRYOVALVE SG PULMONARY HUMAN HEART VALVE (AND CONDUIT) (K092021)Cryolife, Inc.2010-05-25