meddevicedb.com FDA Device Reference

PROCERA ABUTMENT OCTAGON

K041275 Class II Traditional
Decision Date
2004-05-27
Sponsor / Applicant
Nobel Biocare Uas, Inc.

Technical Specification

510(k) Submission ID K041275
Product Code NHA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3630
Decision Date 2004-05-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PROCERA ABUTMENT OCTAGON received FDA 510(k) clearance under submission number K041275, sponsored by Nobel Biocare Uas, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2004-05-27.

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.