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UPPER EXTREMITY TRACTION DEVICE

K803021 Class I Traditional
Decision Date
1980-12-12
Sponsor / Applicant
Orthopedic Systems, Inc.

Technical Specification

510(k) Submission ID K803021
Product Code HST
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.5850
Decision Date 1980-12-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UPPER EXTREMITY TRACTION DEVICE received FDA 510(k) clearance under submission number K803021, sponsored by Orthopedic Systems, 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 1980-12-12.

Classification & Regulation

This clearance is catalogued under FDA product code HST and 21 CFR 888.5850, within the Orthopedic review panel as a Class I device.