Clearance Summary
CG FUTURE ANNULOPLASTY BAND received FDA 510(k) clearance under submission number K052860, sponsored by Medtronic Heart Valves. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2005-11-10.
- Submission: K052860
- Applicant / Sponsor: Medtronic Heart Valves
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.3800
- Decision date: 2005-11-10
Classification & Regulation
This clearance is catalogued under FDA product code KRH and 21 CFR 870.3800, within the Cardiovascular review panel as a Class II device.