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OSSEOLINK DENTAL IMPLANT SYSTEM

K091878 Class II Traditional
Decision Date
2009-10-06
Sponsor / Applicant
Global Implant Solutions, LLC

Technical Specification

510(k) Submission ID K091878
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 2009-10-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OSSEOLINK DENTAL IMPLANT SYSTEM received FDA 510(k) clearance under submission number K091878, sponsored by Global Implant Solutions, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2009-10-06.

Classification & Regulation

This clearance is catalogued under FDA product code DZE and 21 CFR 872.3640, within the Dental review panel as a Class II device.