meddevicedb.com FDA Device Reference

P.004 ABUTMENTS

K072679 Class II Special
Decision Date
2007-10-12
Sponsor / Applicant
Institut Straumann AG

Technical Specification

510(k) Submission ID K072679
Product Code NHA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3630
Decision Date 2007-10-12
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

P.004 ABUTMENTS received FDA 510(k) clearance under submission number K072679, 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 2007-10-12.

Classification & Regulation

This clearance is catalogued under FDA product code NHA and 21 CFR 872.3630, within the Dental review panel as a Class II device.