Atlas FDA

CARDIOGENESIS TMR SYSTEM

FDA premarket approval P970029/S018 · decided 2011-12-16

Approval details

PMA number
P970029
Supplement
S018
Supplement type
30-Day Notice
Trade name
CARDIOGENESIS TMR SYSTEM
Generic name
SYSTEM, LASER, TRANSMYOCARDIAL REVASCULARIZATION
Applicant
Cryolife, Inc.
Date received
2011-11-17
Decision date
2011-12-16
Days to decision
29 days
Decision code
OK30
Product code
MNO
Advisory committee
Cardiovascular
Expedited review
No
Location
Kennesaw, GA
Statement
CHANGES TO THE MANUFACTURING OF THE HANDPIECE DELIVERY SYSTEM.

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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