FDA 510(k) Applications Submitted by JEREMY MARKOVICH

FDA 510(k) Number Submission Date Device Name Applicant
K140319 02/10/2014 COROENT TI-C SYSTEM NUVASIVE, INC.
K180480 02/23/2018 ATEC Universal Spacer System Alphatec Spine, Inc
K140563 03/05/2014 LATERAL VBR SYSTEM NUVASIVE, INCORPORATED
K130820 03/25/2013 EXPANDABLE LUMBAR INTERBODY SYSTEM NUVASIVE, INCORPORATED
K231611 06/02/2023 HOLO PortalÖ Surgical Guidance System Surgalign Spine Technologies
K131723 06/12/2013 COROENT SINGLE TAB SYSTEM NUVASIVE, INC.
K141665 06/23/2014 NuVasive CoRoent System NUVASIVE, INC.
K101977 07/14/2010 TAPERED SCREW-VENT T IMPLANT ZIMMER DENTAL INC.
K141968 07/21/2014 NUVASIVE NVM5 SYSTEM NUVASIVE, INC.
K181980 07/25/2018 OsseoScrew System Alphatec Spine, Inc.
K112160 07/27/2011 TAPERED SCREW-VENT X IMPLANT ZIMMER DENTAL INC.
K182617 09/24/2018 ATEC IOM Accessory Instruments Alphatec Spine, Inc
K113092 10/19/2011 ZIMMER CONTOUR PROVISIONAL COPING ZIMMER DENTAL INC.
K133530 11/15/2013 NUVASIVE EMG ENDOTRACHEAL TUBE NUVASIVE, INCORPORATED
K143641 12/22/2014 NuVasive NVM5 System NuVasive, Incorporated


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