Atlas FDA

ECLIPSE TMR HOLMIUN LASER SYSTEM

FDA premarket approval P970029/S003 · decided 2000-03-22

Approval details

PMA number
P970029
Supplement
S003
Supplement type
Special (Immediate Track)
Supplement reason
Change Design/Components/Specifications/Material
Trade name
ECLIPSE TMR HOLMIUN LASER SYSTEM
Generic name
SYSTEM, LASER, TRANSMYOCARDIAL REVASCULARIZATION
Applicant
Cryolife, Inc.
Date received
1999-12-06
Decision date
2000-03-22
Days to decision
107 days
Decision code
APPR
Product code
MNO
Advisory committee
Cardiovascular
Expedited review
No
Location
Kennesaw, GA
Statement
Approval of a new test fiber and four new labels.

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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