Clearance Summary
IMPLANTECH JEJ PERI-PYRIFORM IMPLANT received FDA 510(k) clearance under submission number K962824, sponsored by Implantech Associates, Inc.. 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 1996-10-03.
- Submission: K962824
- Applicant / Sponsor: Implantech Associates, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.3680
- Decision date: 1996-10-03
Classification & Regulation
This clearance is catalogued under FDA product code FZE and 21 CFR 878.3680, within the General, Plastic Surgery review panel as a Class II device.