FDA 510(k) Applications Submitted by BRIAN J BERGERON

FDA 510(k) Number	Submission Date	Device Name	Applicant
K161438	05/24/2016	Genesys Spine Apache« Anterior Lumbar Interbody Fusion System	GENESYS SPINE
K222798	09/16/2022	Rejoni Intrauterine Catheter	Rejoni, Inc.
K111132	04/22/2011	GENESYS SPINE ANTERIOR CERVICAL PLATE SYSTEM	GENESYS SPINE
K103671	12/16/2010	GENESYS SPINE TILOCK SYSTEM	GENESYS SPINE
K133911	12/23/2013	GENESYS SPINE ANTERIOR BUTTRESS PLATE SYSTEM	GENESYS SPINE
K181124	04/30/2018	Acessa ProVu System	Acessa Health, Inc.
K171656	06/05/2017	Genesys Spine Apache Interbody Fusion System	Genesys Spine
K172469	08/15/2017	TiLock Modular Spinal System	Genesys Spine
K173885	12/21/2017	Genesys Spine Binary Lumbar Plate System	Genesys Spine