FDA 510(k) Applications Submitted by NOAH J BARTSCH

FDA 510(k) Number Submission Date Device Name Applicant
K050121 01/19/2005 ZIMMER PERIARTICULAR LOCKING PLATE SYSTEM, MODEL 2357 & 2359 ZIMMER, INC.
DEN160006 02/03/2016 everlinQ endoAVF System TVA Medical, Inc.
K090507 02/25/2009 MODIFICATION TO LDR SPINE ROI INTERBODY FUSION SYSTEM; ROI-A IMPLANT SYSTEM LDR SPINE USA
K080569 02/29/2008 LDR SPINE ROI-T IMPLANT LDR SPINE USA
K080572 02/29/2008 LDR SPINE ROI-A IMPLANT LDR SPINE USA
K100575 03/01/2010 LDR SPINE USA SPINE TUNE TL SPINE SYSTEM LDR SPINE USA
K060634 03/09/2006 NEX-LINK SPINAL FIXATION SYSTEM ROD TO ROD CONNECTORS, MODELS 725, 726 SERIES ABBOTT SPINE, INC.
K080728 03/14/2008 LDR SPINE ROI-C IMPLANT LDR SPINE USA
K050706 03/18/2005 HARMONY PORT SYSTEM, MODEL 1907 SERIES SPINAL CONCEPTS, INC.
K091088 04/15/2009 LDR SPINE CERVICAL INTERBODY FUSION SYSTEM LDR SPINE USA
K051000 04/20/2005 FORTITUDE VUE VERTEBRAL BODY REPLACEMENT DEVICE SPINAL CONCEPTS, INC.
K052072 08/01/2005 THE SC-ACUFIX ANT-CER DYNAMIC CERVICAL PLATE SYSTEM SINGLE LEVEL PLATES ABBOTT SPINE, INC.
K052247 08/18/2005 NEX-LINK SPINAL FIXATION SYSTEM VARIABLE CROSSLINK, MODEL 721-XX ABBOTT SPINE, INC.
K062505 08/28/2006 NEX-LINK SPINAL FIXATION SYSTEM OFFSET CONNECTORS, 2121-XX SERIES ABBOTT SPINE, INC.
K082592 09/08/2008 LDR SPINE EASYSPINE SYSTEM LDR SPINE USA
K052566 09/19/2005 NEX-LINK SPINAL FIXATION SYSTEM OPEN POLYAXIAL SCREWS, MODELS 2112, 2113, 2118, 2119, 2120. NEX-LINK SPINAL FIXATION SY ABBOTT SPINE, INC.
K042598 09/23/2004 PERIARTICULAR LOCKING PLATES AND SCREWS, 2357 AND 2359 SERIES ZIMMER, INC.
K042761 10/05/2004 WRISTORE DISTAL RADIUS FRACTURE FIXATOR, 4600 SERIES ZIMMER, INC.
K043227 11/22/2004 PERIARTICULAR LOCKING PLATES, 2358 SERIES ZIMMER, INC.
K083857 12/24/2008 LDR SPINE ROI-C IMPLANT LDR SPINE USA
K040389 02/17/2004 COONRAD/MORREY ELBOW CEMENT RESTRICTOR ZIMMER, INC.


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