meddevicedb.com FDA Device Reference

AltiVate Anatomic Shoulder System

K162024 Class II Traditional
Decision Date
2016-11-21
Sponsor / Applicant
Encore Medical L.P.

Technical Specification

510(k) Submission ID K162024
Product Code KWS
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3660
Decision Date 2016-11-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AltiVate Anatomic Shoulder System received FDA 510(k) clearance under submission number K162024, sponsored by Encore Medical L.P.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2016-11-21.

Classification & Regulation

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