FDA 510(k) Applications Submitted by STACEY BONNELL

FDA 510(k) Number	Submission Date	Device Name	Applicant
K130146	01/22/2013	SYNTHES SYNFLATE VERTEVRAL BALLOON SYSTEM	SYNTHES (USA) LLC
K090549	03/02/2009	SYNTHES SYNAPSE TRANSCONNECTOR	SYNTHES SPINE
K211051	04/08/2021	DePuy Synthes 2.7mm Straight and 2.7mm Adaption Plates (Modular Mini Fragment LCP System)	DePuy Synthes
K091159	04/21/2009	SYNTHES ORACLE PLATE	SYNTHES SPINE
K201321	05/18/2020	DePuy Synthes 2.7mm VA LCP Clavicle Plate System	DePuy Synthes
K161417	05/23/2016	DePuy Synthes MAXFRAME Multi-Axial Correction System	SYNTHES USA, LLC
K091689	06/10/2009	SYNAPSE SYSTEM 4.0MM, OC FUSION SYSTEM 4.0MM	SYNTHES (USA)
K071667	06/19/2007	SYNTHES VECTRA-ONE SYSTEM	SYNTHES SPINE
K201959	07/14/2020	DePuy Synthes 2.7mm VA LCP Clavicle Hook Plate System	DePuy Synthes
K112068	07/20/2011	SYNTHES ZERO-P VARIABLE ANGLE (VA)	SYNTHES SPINE CO.LP
K112459	08/26/2011	SYNTHES ZERO-P	SYNTHES SPINE CO.LP
K072791	10/01/2007	ORACLE SPACER, OPAL SPACER	SYNTHES SPINE
K203414	11/19/2020	DePuy Synthes 2.7mm VA LCP Clavicle Plate System, DePuy Synthes 2.7mm VA LCP Clavicle Hook Plate System	DePuy Synthes