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HA-BIONTEGRATED DENTAL IMPLANT SYSTEMS

K914137 Class II Traditional
Decision Date
1994-02-03
Sponsor / Applicant
Lifecore Biomedical, Inc.

Technical Specification

510(k) Submission ID K914137
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 1994-02-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HA-BIONTEGRATED DENTAL IMPLANT SYSTEMS received FDA 510(k) clearance under submission number K914137, sponsored by Lifecore Biomedical, 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 1994-02-03.

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.