meddevicedb.com FDA Device Reference

OBSIDIAN CERAMIC BLOCKS

K100781 Class II Abbreviated
Decision Date
2010-06-21
Sponsor / Applicant
Prismatik Dentalcraft, Inc.

Technical Specification

510(k) Submission ID K100781
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 2010-06-21
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OBSIDIAN CERAMIC BLOCKS received FDA 510(k) clearance under submission number K100781, sponsored by Prismatik Dentalcraft, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2010-06-21.

Classification & Regulation

This clearance is catalogued under FDA product code EIH and 21 CFR 872.6660, within the Dental review panel as a Class II device.