meddevicedb.com FDA Device Reference

PERIOSTEAL ELEVATOR

K771747 Class I Traditional
Decision Date
1977-09-28
Sponsor / Applicant
Depuy, Inc.

Technical Specification

510(k) Submission ID K771747
Product Code EMJ
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4565
Decision Date 1977-09-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PERIOSTEAL ELEVATOR received FDA 510(k) clearance under submission number K771747, sponsored by Depuy, 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 1977-09-28.

Classification & Regulation

This clearance is catalogued under FDA product code EMJ and 21 CFR 872.4565, within the Dental review panel as a Class I device.