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ENDOSSEOUS DENTAL IMPLANT

K113113 Class II Traditional
Decision Date
2012-11-16
Sponsor / Applicant
Ot Medical GmbH

Technical Specification

510(k) Submission ID K113113
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 2012-11-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENDOSSEOUS DENTAL IMPLANT received FDA 510(k) clearance under submission number K113113, sponsored by Ot Medical GmbH. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2012-11-16.

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.