meddevicedb.com FDA Device Reference

ACUMED ANATOMIC RADIAL HEAD SYSTEM

K041858 Class II Traditional
Decision Date
2004-10-05
Sponsor / Applicant
Acumed, LLC

Technical Specification

510(k) Submission ID K041858
Product Code KWI
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3170
Decision Date 2004-10-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACUMED ANATOMIC RADIAL HEAD SYSTEM received FDA 510(k) clearance under submission number K041858, sponsored by Acumed, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2004-10-05.

Classification & Regulation

This clearance is catalogued under FDA product code KWI and 21 CFR 888.3170, within the Orthopedic review panel as a Class II device.