meddevicedb.com FDA Device Reference

OPTICAL CATHETER ARTHROSCOPE

K911296 Class II Traditional
Decision Date
1991-09-24
Sponsor / Applicant
Medical Dynamics, Inc.

Technical Specification

510(k) Submission ID K911296
Product Code HRX
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.1100
Decision Date 1991-09-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OPTICAL CATHETER ARTHROSCOPE received FDA 510(k) clearance under submission number K911296, sponsored by Medical Dynamics, 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 1991-09-24.

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.