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MODIFICATION TO: XIVE 3.0 DENTAL IMPLANT SYSTEM, MULTIPLE

K032750 Class II Special
Decision Date
2003-10-02
Sponsor / Applicant
Friandent GmbH

Technical Specification

510(k) Submission ID K032750
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 2003-10-02
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODIFICATION TO: XIVE 3.0 DENTAL IMPLANT SYSTEM, MULTIPLE received FDA 510(k) clearance under submission number K032750, sponsored by Friandent GmbH. The device was reviewed via the Special premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2003-10-02.

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.