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TSV BellaTek Encode Healing Abutments

K173374 Class II Traditional
Decision Date
2017-12-13
Sponsor / Applicant
Biomet 3i

Technical Specification

510(k) Submission ID K173374
Product Code NHA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3630
Decision Date 2017-12-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TSV BellaTek Encode Healing Abutments received FDA 510(k) clearance under submission number K173374, sponsored by Biomet 3i. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2017-12-13.

Classification & Regulation

This clearance is catalogued under FDA product code NHA and 21 CFR 872.3630, within the Dental review panel as a Class II device.