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ADAPTABLE COMPOSITE RESIN RESTORATIVE MATERIAL

K083841 Class II Traditional
Decision Date
2009-04-14
Sponsor / Applicant
Dentsply International, Inc.

Technical Specification

510(k) Submission ID K083841
Product Code EBF
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3690
Decision Date 2009-04-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ADAPTABLE COMPOSITE RESIN RESTORATIVE MATERIAL received FDA 510(k) clearance under submission number K083841, sponsored by Dentsply International, 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 2009-04-14.

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.