meddevicedb.com FDA Device Reference

GLOBAL UNITE™ Platform Shoulder System

K212710 Class II Special
Decision Date
2021-09-15
Sponsor / Applicant
Depuy Ireland UC

Technical Specification

510(k) Submission ID K212710
Product Code PHX
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3660
Decision Date 2021-09-15
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GLOBAL UNITE™ Platform Shoulder System received FDA 510(k) clearance under submission number K212710, sponsored by Depuy Ireland UC. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2021-09-15.

Classification & Regulation

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