Clearance Summary
LAD, MODEL LAD-01 received FDA 510(k) clearance under submission number K021222, sponsored by Norwood Abbey , 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 2003-01-08.
- Submission: K021222
- Applicant / Sponsor: Norwood Abbey , Ltd.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4810
- Decision date: 2003-01-08
Classification & Regulation
This clearance is catalogued under FDA product code GEX and 21 CFR 878.4810, within the General, Plastic Surgery review panel as a Class II device.