FDA 510(k), K213815, SiJoin®T3

510(K) Number: K213815
Device Name: SiJoin®T3
Manufacturer: VGI Medical, Inc.
Device Classification Name: Sacroiliac Joint Fixation
Regulation Number: 888.3040
Classification Product Code: OUR
Date Received: 12/07/2021
Decision Date: 03/29/2023
Regulation Medical Specialty: Orthopedic

208 pages (2,514 of 2,722 original pages are fully redacted)