meddevicedb.com FDA Device Reference

Medacta Anatomic Shoulder Prosthesis

K170910 Class II Traditional
Decision Date
2017-08-16
Sponsor / Applicant
Medacta International S.A.

Technical Specification

510(k) Submission ID K170910
Product Code KWS
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3660
Decision Date 2017-08-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Medacta Anatomic Shoulder Prosthesis received FDA 510(k) clearance under submission number K170910, sponsored by Medacta International S.A.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2017-08-16.

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.