meddevicedb.com FDA Device Reference

Total Wrist Arthroplasty System (TWA)

K243381 Class II Special
Decision Date
2024-11-01
Sponsor / Applicant
Skeletal Dynamics, Inc.

Technical Specification

510(k) Submission ID K243381
Product Code JWJ
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3800
Decision Date 2024-11-01
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Total Wrist Arthroplasty System (TWA) received FDA 510(k) clearance under submission number K243381, sponsored by Skeletal Dynamics, 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 2024-11-01.

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.