FDA 510(k), K211785, CASSATT™ SIJ Fixation System

FDA 510(k), K211785, CASSATT™ SIJ Fixation System

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510(K) Number: K211785
Device Name: CASSATT™ SIJ Fixation System
Manufacturer: CTL Medical Corporation
Device Classification Name: Sacroiliac Joint Fixation
Regulation Number: 888.3040
Classification Product Code: OUR
Date Received: 06/09/2021
Decision Date: 10/17/2022
Regulation Medical Specialty: Orthopedic

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