Clearance Summary
ASCENDX VCF REDUCTION SYSTEM received FDA 510(k) clearance under submission number K100404, sponsored by Aoi Medical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2012-12-14.
- Submission: K100404
- Applicant / Sponsor: Aoi Medical, Inc.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3027
- Decision date: 2012-12-14
Classification & Regulation
This clearance is catalogued under FDA product code NDN and 21 CFR 888.3027, within the Orthopedic review panel as a Class II device.