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Aequalis Ascend Flex Shoulder System

K190521 Class II Special
Decision Date
2019-06-12
Sponsor / Applicant
Tornier S.A.S.

Technical Specification

510(k) Submission ID K190521
Product Code KWS
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3660
Decision Date 2019-06-12
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Aequalis Ascend Flex Shoulder System received FDA 510(k) clearance under submission number K190521, sponsored by Tornier S.A.S.. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2019-06-12.

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.