meddevicedb.com FDA Device Reference

Smart SPACE Shoulder System

K202454 Class II Traditional
Decision Date
2020-12-28
Sponsor / Applicant
Techmah Medical, LLC

Technical Specification

510(k) Submission ID K202454
Product Code QHE
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3660
Decision Date 2020-12-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Smart SPACE Shoulder System received FDA 510(k) clearance under submission number K202454, sponsored by Techmah Medical, 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 2020-12-28.

Classification & Regulation

This clearance is catalogued under FDA product code QHE and 21 CFR 888.3660, within the Orthopedic review panel as a Class II device.