Clearance Summary
PILLING WECK SURGICAL AORTIC SPOON-JAW CLAMP received FDA 510(k) clearance under submission number K992174, sponsored by Pilling Weck Surgical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2000-03-23.
- Submission: K992174
- Applicant / Sponsor: Pilling Weck Surgical
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.4450
- Decision date: 2000-03-23
Classification & Regulation
This clearance is catalogued under FDA product code DXC and 21 CFR 870.4450, within the Cardiovascular review panel as a Class II device.