FDA 510(k) Applications Submitted by Andrew Rogers

FDA 510(k) Number	Submission Date	Device Name	Applicant
K190193	02/04/2019	SpineEX Sagittae« Lateral Lumbar Interbody Fusion Devices	SpineEX Inc.
K200816	03/30/2020	SpineEX Sagittae Lateral Lumbar Interbody Fusion Devices	SpineEX, Inc.
K181531	06/11/2018	SpineEX Sagittae Lateral Lumbar Interbody Fusion Devices	SpineEX Inc.
K223065	09/30/2022	Adcura« Sagittae« Lateral Lumbar Interbody Fusion Devices	Adcura, Inc.
K961120	03/21/1996	MARKER SYSTEM FOR STEREOTAXIC NAVIGATION	HOWMEDICA LEIBINGER, INC.
K961719	05/02/1996	EPITEC TITANIUM IMPLANT SYSTEM FOR THE SURGICAL ANCHORING OF FACIAL PROSTHESES	HOWMEDICA LEIBINGER, INC.
K963030	08/05/1996	LEIBINGER IMF SCREW	HOWMEDICA LEIBINGER, INC.
K954030	08/28/1995	BONE-LOCK	LEIBINGER GMBH
K963739	09/17/1996	LEIBINGER - LUHR SMALL ORTHOPEDIC BONE SCREWS	HOWMEDICA LEIBINGER, INC.
K963740	09/17/1996	LEIBINGER - LUHR SMALL MANDIBULAR BONE SCREWS	HOWMEDICA LEIBINGER, INC.
K963741	09/17/1996	LEIBINGER LUHR SMALL CRANIOMAXILLOFACIAL BONE SCREWS	HOWMEDICA LEIBINGER, INC.