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BIODENTA DENTAL IMPLANT SYSTEM- BONE LEVEL TAPERED

K123415 Class II Traditional
Decision Date
2013-03-19
Sponsor / Applicant
Biodenta Swiss AG

Technical Specification

510(k) Submission ID K123415
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 2013-03-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIODENTA DENTAL IMPLANT SYSTEM- BONE LEVEL TAPERED received FDA 510(k) clearance under submission number K123415, sponsored by Biodenta Swiss AG. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2013-03-19.

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.