meddevicedb.com FDA Device Reference

Trifore(tm) Cervical Plating System

K171112 Class II Traditional
Decision Date
2017-06-08
Sponsor / Applicant
Neurostructures, Inc.

Technical Specification

510(k) Submission ID K171112
Product Code KWQ
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3060
Decision Date 2017-06-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Trifore(tm) Cervical Plating System received FDA 510(k) clearance under submission number K171112, sponsored by Neurostructures, 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 2017-06-08.

Classification & Regulation

This clearance is catalogued under FDA product code KWQ and 21 CFR 888.3060, within the Orthopedic review panel as a Class II device.