meddevicedb.com FDA Device Reference

KLOCKNER DENTAL IMPLANT ABUTMENTS

K122988 Class II Abbreviated
Decision Date
2013-07-19
Sponsor / Applicant
SOADCO, S.L.

Technical Specification

510(k) Submission ID K122988
Product Code NHA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3630
Decision Date 2013-07-19
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

KLOCKNER DENTAL IMPLANT ABUTMENTS received FDA 510(k) clearance under submission number K122988, sponsored by SOADCO, S.L.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2013-07-19.

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.