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P.0004 IMPLANTS

K062129 Class II Special
Decision Date
2006-10-20
Sponsor / Applicant
Institut Straumann AG

Technical Specification

510(k) Submission ID K062129
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 2006-10-20
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

P.0004 IMPLANTS received FDA 510(k) clearance under submission number K062129, sponsored by Institut Straumann AG. The device was reviewed via the Special premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2006-10-20.

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.