meddevicedb.com FDA Device Reference

EZ Plate

K173306 Class II Traditional
Decision Date
2018-01-22
Sponsor / Applicant
Zavation Medical Products, LLC

Technical Specification

510(k) Submission ID K173306
Product Code KWQ
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3060
Decision Date 2018-01-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EZ Plate received FDA 510(k) clearance under submission number K173306, sponsored by Zavation Medical Products, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2018-01-22.

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.