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OSTEOMED BIORESORBABLE FIXATION SYSTEM

K012486 Class II Traditional
Decision Date
2002-01-16
Sponsor / Applicant
Osteomed Corp.

Technical Specification

510(k) Submission ID K012486
Product Code DZL
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4880
Decision Date 2002-01-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OSTEOMED BIORESORBABLE FIXATION SYSTEM received FDA 510(k) clearance under submission number K012486, sponsored by Osteomed Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2002-01-16.

Classification & Regulation

This clearance is catalogued under FDA product code DZL and 21 CFR 872.4880, within the Dental review panel as a Class II device.