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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