meddevicedb.com FDA Device Reference

BTI Dental Implant System UnicCa

K173257 Class II Traditional
Decision Date
2018-08-17
Sponsor / Applicant
B.T.I. Biotechnology Institute, Sl.

Technical Specification

510(k) Submission ID K173257
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 2018-08-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BTI Dental Implant System UnicCa received FDA 510(k) clearance under submission number K173257, sponsored by B.T.I. Biotechnology Institute, Sl.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2018-08-17.

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.