meddevicedb.com FDA Device Reference

DARCO FORCE TITANIUM COMPRESSION SCREW

K062103 Class II Traditional
Decision Date
2006-10-25
Sponsor / Applicant
Darco International, Inc.

Technical Specification

510(k) Submission ID K062103
Product Code HWC
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3040
Decision Date 2006-10-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DARCO FORCE TITANIUM COMPRESSION SCREW received FDA 510(k) clearance under submission number K062103, sponsored by Darco International, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2006-10-25.

Classification & Regulation

This clearance is catalogued under FDA product code HWC and 21 CFR 888.3040, within the Orthopedic review panel as a Class II device.