meddevicedb.com FDA Device Reference

MASTERGRAFT RESORBABLE CERAMIC GRANULES

K082917 Class II Traditional
Decision Date
2009-01-09
Sponsor / Applicant
Medtronic Sofamor Danek

Technical Specification

510(k) Submission ID K082917
Product Code LYC
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3930
Decision Date 2009-01-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MASTERGRAFT RESORBABLE CERAMIC GRANULES received FDA 510(k) clearance under submission number K082917, sponsored by Medtronic Sofamor Danek. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2009-01-09.

Classification & Regulation

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