Clearance Summary
ETHICON ENDO-SURGERY GENERATOR G11, MODEL GEN11 received FDA 510(k) clearance under submission number K101990, sponsored by Ethicon Endo-Sugery, LLC. 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 2011-06-13.
- Submission: K101990
- Applicant / Sponsor: Ethicon Endo-Sugery, LLC
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4400
- Decision date: 2011-06-13
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.