meddevicedb.com FDA Device Reference

ORTHOPEDIC FIXATION DEVICES

K821566 Class II Traditional
Decision Date
1982-06-03
Sponsor / Applicant
Howmedica Corp.

Technical Specification

510(k) Submission ID K821566
Product Code KTW
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 1982-06-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ORTHOPEDIC FIXATION DEVICES received FDA 510(k) clearance under submission number K821566, sponsored by Howmedica Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1982-06-03.

Classification & Regulation

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