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AEQUALIS SHOULDER FRACTURE SYSTEM

K032679 Class II Special
Decision Date
2003-12-15
Sponsor / Applicant
Tornier

Technical Specification

510(k) Submission ID K032679
Product Code KWS
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3660
Decision Date 2003-12-15
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AEQUALIS SHOULDER FRACTURE SYSTEM received FDA 510(k) clearance under submission number K032679, 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 2003-12-15.

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.