meddevicedb.com FDA Device Reference

DSM Biomedical Porcine Pericardium Dental Membrane

K160474 Class II Traditional
Decision Date
2016-06-07
Sponsor / Applicant
Kensey Nash Corporation Dba Dsm Biomedical

Technical Specification

510(k) Submission ID K160474
Product Code NPL
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3930
Decision Date 2016-06-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DSM Biomedical Porcine Pericardium Dental Membrane received FDA 510(k) clearance under submission number K160474, sponsored by Kensey Nash Corporation Dba 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 2016-06-07.

Classification & Regulation

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