Clearance Summary
TRAUMAFUSE PERFUSION PRESSURE RELIEF VALVE received FDA 510(k) clearance under submission number K894721, sponsored by The Traumafuse Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1989-10-20.
- Submission: K894721
- Applicant / Sponsor: The Traumafuse Co.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.4390
- Decision date: 1989-10-20
Classification & Regulation
This clearance is catalogued under FDA product code DWE and 21 CFR 870.4390, within the Cardiovascular review panel as a Class II device.