meddevicedb.com FDA Device Reference

BIO-EYE HYDROXYAPATITE OCULAR IMPLAND AND CONFORMER

K982562 Class II Traditional
Decision Date
1998-12-28
Sponsor / Applicant
Integrated Orbital Implants, Inc.

Technical Specification

510(k) Submission ID K982562
Product Code HPZ
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.3320
Decision Date 1998-12-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIO-EYE HYDROXYAPATITE OCULAR IMPLAND AND CONFORMER received FDA 510(k) clearance under submission number K982562, sponsored by Integrated Orbital Implants, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1998-12-28.

Classification & Regulation

This clearance is catalogued under FDA product code HPZ and 21 CFR 886.3320, within the Ophthalmic review panel as a Class II device.