meddevicedb.com FDA Device Reference

DISTAL RADIUS LOCKING PLATING SYSTEM

K061917 Class II Traditional
Decision Date
2006-08-28
Sponsor / Applicant
Newclip Technics

Technical Specification

510(k) Submission ID K061917
Product Code HRS
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 2006-08-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DISTAL RADIUS LOCKING PLATING SYSTEM received FDA 510(k) clearance under submission number K061917, sponsored by Newclip Technics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2006-08-28.

Classification & Regulation

This clearance is catalogued under FDA product code HRS and 21 CFR 888.3030, within the Orthopedic review panel as a Class II device.