meddevicedb.com FDA Device Reference

Freedom Wrist Arthroplasty System

K233674 Class II Traditional
Decision Date
2024-05-30
Sponsor / Applicant
Ascension Orthopedics, Inc.

Technical Specification

510(k) Submission ID K233674
Product Code JWJ
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3800
Decision Date 2024-05-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Freedom Wrist Arthroplasty System received FDA 510(k) clearance under submission number K233674, sponsored by Ascension Orthopedics, 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 2024-05-30.

Classification & Regulation

This clearance is catalogued under FDA product code JWJ and 21 CFR 888.3800, within the Orthopedic review panel as a Class II device.