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SPECTRANETICS CVX-300 EXCIMER LASER CORONARY ANGIOPLASTY (ELCA) SYSTEM

FDA premarket approval P910001/S026 · decided 2007-05-11

Approval details

PMA number
P910001
Supplement
S026
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
SPECTRANETICS CVX-300 EXCIMER LASER CORONARY ANGIOPLASTY (ELCA) SYSTEM
Generic name
DEVICE, ANGIOPLASTY, LASER, CORONARY
Applicant
Spectranetics Corp.
Date received
2006-11-16
Decision date
2007-05-11
Days to decision
176 days
Decision code
APPR
Product code
LPC
Advisory committee
Cardiovascular
Expedited review
No
Location
Colorado Springs, CO
Statement
APPROVAL FOR THE REMOVAL OF A COATING ON THE INNER LUMEN OF THE EXTREME CATHETER MODEL NUMBERS 114-001, 117-002, AND 120-001, THE CHANGE TO BLACK TUBING FOR 0.9 MM CATHETER MODEL NUMBERS 110-003 AND 110-004 X-80, AND THE CHANGE IN THE STRAIN RELIEF MATERIAL DUROMETER FOR THE 0.9 MM EXTREME CATHETER MODEL NUMBERS 110-001, 110-002, 110-152 AND 0.7 MM EXTREME CATHETER MODEL 110-005 TO PREVENT KINKING AT THE STRAIN RELIEF.

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