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AEQUALIS SHOULDER SYSTEM

K041339 Class II Special
Decision Date
2004-06-17
Sponsor / Applicant
Tornier

Technical Specification

510(k) Submission ID K041339
Product Code KWS
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3660
Decision Date 2004-06-17
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AEQUALIS SHOULDER SYSTEM received FDA 510(k) clearance under submission number K041339, sponsored by Tornier. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2004-06-17.

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.