Clearance Summary
IVAS 10MM AND 15MM BALLOON CATHETER received FDA 510(k) clearance under submission number K130430, sponsored by Stryker Corporation. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2013-05-23.
- Submission: K130430
- Applicant / Sponsor: Stryker Corporation
- Clearance pathway: Special
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.1100
- Decision date: 2013-05-23
Classification & Regulation
This clearance is catalogued under FDA product code HRX and 21 CFR 888.1100, within the Orthopedic review panel as a Class II device.