meddevicedb.com FDA Device Reference

STERI-OSS HYDROXYAPATITE-COATED DENTAL IMPLANT

K883373 Class II Traditional
Decision Date
1989-01-13
Sponsor / Applicant
Denar Corp.

Technical Specification

510(k) Submission ID K883373
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 1989-01-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STERI-OSS HYDROXYAPATITE-COATED DENTAL IMPLANT received FDA 510(k) clearance under submission number K883373, sponsored by Denar Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1989-01-13.

Classification & Regulation

This clearance is catalogued under FDA product code DZE and 21 CFR 872.3640, within the Dental review panel as a Class II device.