Clearance Summary
MEDTRONIC ANDOVER MEDICAL SAF-D-FIB MODEL 1220-002 received FDA 510(k) clearance under submission number K903018, sponsored by Medtronic Andover Medical, 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 1990-12-03.
- Submission: K903018
- Applicant / Sponsor: Medtronic Andover Medical, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.5300
- Decision date: 1990-12-03
Classification & Regulation
This clearance is catalogued under FDA product code LDD and 21 CFR 870.5300, within the Cardiovascular review panel as a Class II device.