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OSI O-BALL ABUTMENT HEAD IMPLANTS

K110548 Class II Traditional
Decision Date
2011-07-29
Sponsor / Applicant
Juell Dental

Technical Specification

510(k) Submission ID K110548
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 2011-07-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OSI O-BALL ABUTMENT HEAD IMPLANTS received FDA 510(k) clearance under submission number K110548, sponsored by Juell Dental. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2011-07-29.

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.