meddevicedb.com FDA Device Reference

Anatomical Shoulder System

K193099 Class II Traditional
Decision Date
2020-01-29
Sponsor / Applicant
Zimmer GmbH

Technical Specification

510(k) Submission ID K193099
Product Code PHX
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3660
Decision Date 2020-01-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Anatomical Shoulder System received FDA 510(k) clearance under submission number K193099, 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 2020-01-29.

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.