meddevicedb.com FDA Device Reference

ORTHOGUARD AB ANTIMICROBIAL SLEEVE

K022676 Class II Special
Decision Date
2002-09-23
Sponsor / Applicant
Smith & Nephew, Inc.

Technical Specification

510(k) Submission ID K022676
Product Code JEC
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3040
Decision Date 2002-09-23
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ORTHOGUARD AB ANTIMICROBIAL SLEEVE received FDA 510(k) clearance under submission number K022676, sponsored by Smith & Nephew, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2002-09-23.

Classification & Regulation

This clearance is catalogued under FDA product code JEC and 21 CFR 888.3040, within the Orthopedic review panel as a Class II device.