meddevicedb.com FDA Device Reference

ORTHO. GAS INSUFFLATOR MODEL IN-2 FOR ARTHRO. SURG

K873331 Class II Traditional
Decision Date
1988-02-17
Sponsor / Applicant
Directed Energy, Inc.

Technical Specification

510(k) Submission ID K873331
Product Code HRX
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.1100
Decision Date 1988-02-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ORTHO. GAS INSUFFLATOR MODEL IN-2 FOR ARTHRO. SURG received FDA 510(k) clearance under submission number K873331, sponsored by Directed Energy, 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 1988-02-17.

Classification & Regulation

This clearance is catalogued under FDA product code HRX and 21 CFR 888.1100, within the Orthopedic review panel as a Class II device.