Clearance Summary
POROUS HDPE SURGICAL IMPLANTS, TO BE DISTRIBUTED UNDER VARIOUS TRADEMARKS INCLUDING EPOR, BIOPOR, MINOPOR & P-HDPE received FDA 510(k) clearance under submission number K022665, sponsored by Hohenstein Enterprises, 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 2002-10-09.
- Submission: K022665
- Applicant / Sponsor: Hohenstein Enterprises, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.3500
- Decision date: 2002-10-09
Classification & Regulation
This clearance is catalogued under FDA product code KKY and 21 CFR 878.3500, within the General, Plastic Surgery review panel as a Class II device.