FDA 510(k) Applications Submitted by AMNON TALMOR

FDA 510(k) Number	Submission Date	Device Name	Applicant
K080331	02/06/2008	SYNTHES CRANIOFACIAL PLATE AND SCREW SYSTEM	SYNTHES (USA)
K100634	03/05/2010	SYNTHES MATRIX SYSTEM	SYNTHES (USA)
K181060	04/23/2018	Solitaire 2 and Solitaire Platinum Revascularization Device	Medtronic Neurovascular
K221531	05/26/2022	ClotTriever Thrombectomy System	Inari Medical, Inc.
K081623	06/10/2008	SYNTHES RIB FIXATION SYSTEM	SYNTHES (USA)
K081700	06/17/2008	SYNTHES (USA) STERNAL FIXATION SYSTEM - LINE EXTENSION	SYNTHES (USA)
K071738	06/26/2007	EXACTECH OPTETRAK PROXIMAL TIBIAL SPACER	EXACTECH, INC.
K211990	06/28/2021	Rist 071 Radial Access Guide Catheter	Micro Therapeutics, Inc., d/b/a ev3 Neurovascular
K062273	08/07/2006	SPACER-G TEMPORARY HIP PROSTHESIS	TECRES SPA
K082335	08/14/2008	SYNTHES MATRIXMANDIBLE PLATE AND SCREW SYSTEM	SYNTHES (USA)
K162760	09/30/2016	Spine Wave Anterior Cervical Spine System	SPINE WAVE, INC.
K083439	11/20/2008	SYNTHES EPOCA SHOULDER PROSTHESIS SYSTEM	SYNTHES (USA)
K063569	11/29/2006	EQUINOXE REVERSE SHOULDER SYSTEM	EXACTECH, INC.
K093762	12/07/2009	SYNTHES ZERO-P	SYNTHES SPINE