meddevicedb.com FDA Device Reference

Cable-Ready Cable Grip System: Cable-Ready Bone Plate System

K151716 Class II Traditional
Decision Date
2016-01-28
Sponsor / Applicant
Zimmer, Inc.

Technical Specification

510(k) Submission ID K151716
Product Code HRS
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 2016-01-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Cable-Ready Cable Grip System: Cable-Ready Bone Plate System received FDA 510(k) clearance under submission number K151716, sponsored by Zimmer, 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 2016-01-28.

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.