Healthcare Professionals

CG Future

Annuloplasty System

CG Future Annuloplasty System

The CG Future® Annuloplasty System for mitral valve repair is designed to predictably remodel the annulus to maintain apposition of the anterior and posterior leaflets. Correct annuloplasty ring/band sizing is an important element to achieve a successful repair.


Remodel the Mitral Annulus While Supporting Physiologic Annular Movement

Surgeons can choose between a semi-rigid ring with a flexible anterior segment or a semi-rigid band, based on their preference and their patient’s needs.

The CG Future® COMPOSITE Ring is the first composite ring to offer posterior remodeling while maintaining anterior flexibility. A flexible anterior segment seamlessly connects to the ring's semi-rigid posterior, providing the support needed to dynamically remodel the annulus, thereby allowing physiologic movement throughout the cardiac cycle.

  • Reduced risk for anterior dilatation
  • Unique eyelet design for easy anchoring to the trigones
  • Semi-rigid design offers enough flexibility to allow movement of the mitral annulus during the cardiac cycle.
  • Ease of implant with 20% lower profile.1 The band is ideal for small incisions and minimally invasive procedures where visibility and access to the anterior portion of the mitral annulus may be limited.
  • Considered a benefit for patients with degenerative, ischemic and dilated cardiomyopathic valve disease
  • The CG Future Ring is available in eight sizes ranging from 24 mm to 38 mm
  • The CG Future Band is available in seven sizes ranging from 26 mm to 38 mm

Important Safety Information

Only physicians who have received proper training should use this device.

Adverse events can include: thromboembolic events, dehiscence, hemolysis, stenosis, residual incompetence, heart block, endocarditis, systolic anterior motion, left ventricular outflow tract obstruction, anticoagulant-related bleeding or hemorrhage.

For a complete listing of Indications, Contraindications, Warnings, Precautions and Adverse events, please refer to the Instructions for Use provided with the product.



Data on file. Medtronic, Inc.