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MONTBLANC IMPLANTOLOGY AND OMNIPRATIQUE CONTRA-ANGLES

K090676 Class I Special
Decision Date
2009-05-22
Sponsor / Applicant
Anthogyr

Technical Specification

510(k) Submission ID K090676
Product Code EFA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4200
Decision Date 2009-05-22
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MONTBLANC IMPLANTOLOGY AND OMNIPRATIQUE CONTRA-ANGLES received FDA 510(k) clearance under submission number K090676, sponsored by Anthogyr. The device was reviewed via the Special premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2009-05-22.

Classification & Regulation

This clearance is catalogued under FDA product code EFA and 21 CFR 872.4200, within the Dental review panel as a Class I device.