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BIOCRYL X

K083479 Class II Traditional
Decision Date
2009-02-27
Sponsor / Applicant
Great Lakes Orthodontics, Ltd.

Technical Specification

510(k) Submission ID K083479
Product Code EBI
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3760
Decision Date 2009-02-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIOCRYL X received FDA 510(k) clearance under submission number K083479, sponsored by Great Lakes Orthodontics, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2009-02-27.

Classification & Regulation

This clearance is catalogued under FDA product code EBI and 21 CFR 872.3760, within the Dental review panel as a Class II device.