Clearance Summary
SYMMETRY AORTIC CLIP SYSTEM received FDA 510(k) clearance under submission number K003446, sponsored by St. Jude Medical Cardiovascular Group, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2001-05-21.
- Submission: K003446
- Applicant / Sponsor: St. Jude Medical Cardiovascular Group, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4300
- Decision date: 2001-05-21
Classification & Regulation
This clearance is catalogued under FDA product code NCA and 21 CFR 878.4300, within the General, Plastic Surgery review panel as a Class II device.