Clearance Summary
Voyant 5mm Fusion Device, Voyant Maryland Fusion Device received FDA 510(k) clearance under submission number K193292, sponsored by Applied Medical Resources Corp.. 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 2019-12-20.
- Submission: K193292
- Applicant / Sponsor: Applied Medical Resources Corp.
- Clearance pathway: Special
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4400
- Decision date: 2019-12-20
Classification & Regulation
This clearance is catalogued under FDA product code GEI and 21 CFR 878.4400, within the General, Plastic Surgery review panel as a Class II device.