meddevicedb.com FDA Device Reference

BROOKER EXTERNAL FIXATION FRAME

K840286 Class II Traditional
Decision Date
1984-02-09
Sponsor / Applicant
Depuy, Inc.

Technical Specification

510(k) Submission ID K840286
Product Code JDW
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3040
Decision Date 1984-02-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BROOKER EXTERNAL FIXATION FRAME received FDA 510(k) clearance under submission number K840286, sponsored by Depuy, 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 1984-02-09.

Classification & Regulation

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