FDA 510(k), K213815, SiJoin®T3

FDA 510(k), K213815, SiJoin®T3

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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

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