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TPH Spectra+ Universal Composite Restorative

K162107 Class II Traditional
Decision Date
2016-09-27
Sponsor / Applicant
Dentsply Sirona

Technical Specification

510(k) Submission ID K162107
Product Code EBF
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3690
Decision Date 2016-09-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TPH Spectra+ Universal Composite Restorative received FDA 510(k) clearance under submission number K162107, sponsored by Dentsply Sirona. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2016-09-27.

Classification & Regulation

This clearance is catalogued under FDA product code EBF and 21 CFR 872.3690, within the Dental review panel as a Class II device.