Clearance Summary
2cm Peripheral Cutting Balloon Microsurgical Dilatation Catheter received FDA 510(k) clearance under submission number K151253, sponsored by Boston Scientific Limited. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2015-06-10.
- Submission: K151253
- Applicant / Sponsor: Boston Scientific Limited
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1250
- Decision date: 2015-06-10
Classification & Regulation
This clearance is catalogued under FDA product code PNO and 21 CFR 870.1250, within the Cardiovascular review panel as a Class II device.