Clearance Summary
Renasys Edge received FDA 510(k) clearance under submission number K231939, sponsored by Smith & Nephew Medical, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2024-05-24.
- Submission: K231939
- Applicant / Sponsor: Smith & Nephew Medical, Ltd.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4780
- Decision date: 2024-05-24
Classification & Regulation
This clearance is catalogued under FDA product code OMP and 21 CFR 878.4780, within the General, Plastic Surgery review panel as a Class II device.