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ARTHROBOT 101 UPPER LIMB TRACTION ACCESSORY

K873080 Class I Traditional
Decision Date
1987-11-25
Sponsor / Applicant
Andronic Devices, Ltd.

Technical Specification

510(k) Submission ID K873080
Product Code JEA
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4960
Decision Date 1987-11-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ARTHROBOT 101 UPPER LIMB TRACTION ACCESSORY received FDA 510(k) clearance under submission number K873080, sponsored by Andronic Devices, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1987-11-25.

Classification & Regulation

This clearance is catalogued under FDA product code JEA and 21 CFR 878.4960, within the General, Plastic Surgery review panel as a Class I device.