Clearance Summary
SULZER CARBOMEDICS CARDIOFIX PERICARDIUM received FDA 510(k) clearance under submission number K993288, sponsored by Sulzer Carbomedics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1999-12-29.
- Submission: K993288
- Applicant / Sponsor: Sulzer Carbomedics, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.3470
- Decision date: 1999-12-29
Classification & Regulation
This clearance is catalogued under FDA product code DXZ and 21 CFR 870.3470, within the Cardiovascular review panel as a Class II device.