meddevicedb.com FDA Device Reference

SILICONE SPHERES

K112176 Class II Special
Decision Date
2011-09-15
Sponsor / Applicant
Oculo Plastik, Inc.

Technical Specification

510(k) Submission ID K112176
Product Code HPZ
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.3320
Decision Date 2011-09-15
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SILICONE SPHERES received FDA 510(k) clearance under submission number K112176, sponsored by Oculo Plastik, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2011-09-15.

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.