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INTERLOGICS W-TRACKER AND WRIST WORKS SOFTWARE

K971079 Class I Traditional
Decision Date
1997-07-09
Sponsor / Applicant
Interlogics, Inc.

Technical Specification

510(k) Submission ID K971079
Product Code KQX
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.1500
Decision Date 1997-07-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INTERLOGICS W-TRACKER AND WRIST WORKS SOFTWARE received FDA 510(k) clearance under submission number K971079, sponsored by Interlogics, 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 1997-07-09.

Classification & Regulation

This clearance is catalogued under FDA product code KQX and 21 CFR 888.1500, within the Orthopedic review panel as a Class I device.