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Implantswiss Dental Implant System and Implantswiss Dental Abutment System

K200867 Class II Special
Decision Date
2020-04-28
Sponsor / Applicant
Novodent SA

Technical Specification

510(k) Submission ID K200867
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 2020-04-28
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Implantswiss Dental Implant System and Implantswiss Dental Abutment System received FDA 510(k) clearance under submission number K200867, sponsored by Novodent SA. The device was reviewed via the Special premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2020-04-28.

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.