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OSTEOSORB TACK FIXATION SYSTEM

K030989 Class II Traditional
Decision Date
2004-04-01
Sponsor / Applicant
Noviace Corporation

Technical Specification

510(k) Submission ID K030989
Product Code JEY
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4760
Decision Date 2004-04-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OSTEOSORB TACK FIXATION SYSTEM received FDA 510(k) clearance under submission number K030989, sponsored by Noviace Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2004-04-01.

Classification & Regulation

This clearance is catalogued under FDA product code JEY and 21 CFR 872.4760, within the Dental review panel as a Class II device.