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STAR/VENT INTERNAL HEX SCREW IMPLANT

K082800 Class II Traditional
Decision Date
2010-08-26
Sponsor / Applicant
Park Dental Research Corp.

Technical Specification

510(k) Submission ID K082800
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 2010-08-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STAR/VENT INTERNAL HEX SCREW IMPLANT received FDA 510(k) clearance under submission number K082800, sponsored by Park Dental Research Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2010-08-26.

Classification & Regulation

This clearance is catalogued under FDA product code DZE and 21 CFR 872.3640, within the Dental review panel as a Class II device.