meddevicedb.com FDA Device Reference

Porcine Mineral Collagen Composite

K202183 Class II Traditional
Decision Date
2021-04-02
Sponsor / Applicant
Collagen Matrix, Inc.

Technical Specification

510(k) Submission ID K202183
Product Code NPM
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3930
Decision Date 2021-04-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Porcine Mineral Collagen Composite received FDA 510(k) clearance under submission number K202183, sponsored by Collagen Matrix, 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 2021-04-02.

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.