Clearance Summary
Stimucel System, Stimucel Generator, Stimucel Treatment Wand, Stimucel Applicator received FDA 510(k) clearance under submission number K162721, sponsored by Alliqua Biomedical, Inc.. 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 2016-12-22.
- Submission: K162721
- Applicant / Sponsor: Alliqua Biomedical, Inc.
- Clearance pathway: Special
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4410
- Decision date: 2016-12-22
Classification & Regulation
This clearance is catalogued under FDA product code NRB and 21 CFR 878.4410, within the General, Plastic Surgery review panel as a Class II device.