meddevicedb.com FDA Device Reference

UltraThineer Zirconia Slurry (5Y-B)

K240419 Class II Traditional
Decision Date
2024-04-12
Sponsor / Applicant
Boston Micro Fabrication

Technical Specification

510(k) Submission ID K240419
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 2024-04-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UltraThineer Zirconia Slurry (5Y-B) received FDA 510(k) clearance under submission number K240419, sponsored by Boston Micro Fabrication. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2024-04-12.

Classification & Regulation

This clearance is catalogued under FDA product code EIH and 21 CFR 872.6660, within the Dental review panel as a Class II device.