meddevicedb.com FDA Device Reference

PROMOS MODULAR SHOULDER SYSTEM

K113012 Class II Traditional
Decision Date
2012-01-05
Sponsor / Applicant
Smith & Nephew, Inc.

Technical Specification

510(k) Submission ID K113012
Product Code KWS
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3660
Decision Date 2012-01-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PROMOS MODULAR SHOULDER SYSTEM received FDA 510(k) clearance under submission number K113012, sponsored by Smith & Nephew, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2012-01-05.

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.