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DSM Biomedical Dental Bone Graft Plus

K193212 Class II Traditional
Decision Date
2020-09-10
Sponsor / Applicant
Dsm Biomedical

Technical Specification

510(k) Submission ID K193212
Product Code NPM
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3930
Decision Date 2020-09-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DSM Biomedical Dental Bone Graft Plus received FDA 510(k) clearance under submission number K193212, sponsored by Dsm Biomedical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2020-09-10.

Classification & Regulation

This clearance is catalogued under FDA product code NPM and 21 CFR 872.3930, within the Dental review panel as a Class II device.