Atlas FDA

CARDIOGENESIS TMR LASER SYSTEM

FDA premarket approval P970029/S032 · decided 2016-08-23

Approval details

PMA number
P970029
Supplement
S032
Supplement type
Special (Immediate Track)
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
CARDIOGENESIS TMR LASER SYSTEM
Generic name
SYSTEM, LASER, TRANSMYOCARDIAL REVASCULARIZATION
Applicant
Cryolife, Inc.
Date received
2016-08-12
Decision date
2016-08-23
Days to decision
11 days
Decision code
APPR
Product code
MNO
Advisory committee
Cardiovascular
Expedited review
No
Location
Kennesaw, GA
Statement
Approval for labeling changes to enhance the safety of CardioGenesisĀ® TMR Laser System.

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.

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