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X-2 IMPLANT ABUTMENT; BAR MALE; DISTAL EXTENSION MALE

K042466 Class II Special
Decision Date
2004-11-24
Sponsor / Applicant
Zest Anchors, Inc.

Technical Specification

510(k) Submission ID K042466
Product Code NHA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3630
Decision Date 2004-11-24
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

X-2 IMPLANT ABUTMENT; BAR MALE; DISTAL EXTENSION MALE received FDA 510(k) clearance under submission number K042466, sponsored by Zest Anchors, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2004-11-24.

Classification & Regulation

This clearance is catalogued under FDA product code NHA and 21 CFR 872.3630, within the Dental review panel as a Class II device.