Clearance Summary
FasTouch Fixation System received FDA 510(k) clearance under submission number K162252, sponsored by Via Surgical , Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2016-11-14.
- Submission: K162252
- Applicant / Sponsor: Via Surgical , Ltd.
- Clearance pathway: Special
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4750
- Decision date: 2016-11-14
Classification & Regulation
This clearance is catalogued under FDA product code GDW and 21 CFR 878.4750, within the General, Plastic Surgery review panel as a Class II device.