meddevicedb.com FDA Device Reference

CASSATT™ SIJ Fixation System

K211785 Class II Traditional
Decision Date
2022-10-17
Sponsor / Applicant
Ctl Medical Corporation

Technical Specification

510(k) Submission ID K211785
Product Code OUR
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3040
Decision Date 2022-10-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CASSATT™ SIJ Fixation System received FDA 510(k) clearance under submission number K211785, sponsored by Ctl Medical Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2022-10-17.

Classification & Regulation

This clearance is catalogued under FDA product code OUR and 21 CFR 888.3040, within the Orthopedic review panel as a Class II device.