meddevicedb.com FDA Device Reference

3M MODULAR SHOULDER SYSTEM

K920362 Class II Traditional
Decision Date
1993-07-22
Sponsor / Applicant
3M Health Care, Ltd.

Technical Specification

510(k) Submission ID K920362
Product Code KWS
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3660
Decision Date 1993-07-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

3M MODULAR SHOULDER SYSTEM received FDA 510(k) clearance under submission number K920362, sponsored by 3M Health Care, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1993-07-22.

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.