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PACIFIC IMPLANT TITANIUM ENDODONTIC POINT

K992582 Class I Traditional
Decision Date
1999-10-21
Sponsor / Applicant
Pacific Implant, Inc.

Technical Specification

510(k) Submission ID K992582
Product Code EKL
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3840
Decision Date 1999-10-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PACIFIC IMPLANT TITANIUM ENDODONTIC POINT received FDA 510(k) clearance under submission number K992582, sponsored by Pacific Implant, 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 1999-10-21.

Classification & Regulation

This clearance is catalogued under FDA product code EKL and 21 CFR 872.3840, within the Dental review panel as a Class I device.