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COUPLING DEVICE FOR DENTAL PROSTHESIS

K950259 Class I Traditional
Decision Date
1996-12-06
Sponsor / Applicant
Dr. Joseph E. Grasso, D.D.S.

Technical Specification

510(k) Submission ID K950259
Product Code EGG
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3165
Decision Date 1996-12-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COUPLING DEVICE FOR DENTAL PROSTHESIS received FDA 510(k) clearance under submission number K950259, sponsored by Dr. Joseph E. Grasso, D.D.S.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1996-12-06.

Classification & Regulation

This clearance is catalogued under FDA product code EGG and 21 CFR 872.3165, within the Dental review panel as a Class I device.