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VERTEX SEALAND L/C ORTHODONTIC SEALANT

K010547 Class II Traditional
Decision Date
2001-08-16
Sponsor / Applicant
Apex Dental Materials, Inc.

Technical Specification

510(k) Submission ID K010547
Product Code KLE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3200
Decision Date 2001-08-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VERTEX SEALAND L/C ORTHODONTIC SEALANT received FDA 510(k) clearance under submission number K010547, sponsored by Apex Dental Materials, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2001-08-16.

Classification & Regulation

This clearance is catalogued under FDA product code KLE and 21 CFR 872.3200, within the Dental review panel as a Class II device.