meddevicedb.com FDA Device Reference

ASHCOM Shoulder System, Anatomical Shoulder System and Anatomical Shoulder Combined System

K170711 Class II Traditional
Decision Date
2017-06-01
Sponsor / Applicant
Zimmer GmbH

Technical Specification

510(k) Submission ID K170711
Product Code PHX
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3660
Decision Date 2017-06-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ASHCOM Shoulder System, Anatomical Shoulder System and Anatomical Shoulder Combined System received FDA 510(k) clearance under submission number K170711, sponsored by Zimmer GmbH. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2017-06-01.

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.