FDA 510(k) Applications Submitted by THEKEN SPINE LLC

FDA 510(k) Number Submission Date Device Name Applicant
K070381 02/08/2007 THEKEN VU MESH VBR SYSTEM THEKEN SPINE LLC
K070638 03/07/2007 THEKEN ATOLL CERVICO-THORACIC SYSTEM THEKEN SPINE LLC
K080690 03/11/2008 MANTA RAY ANTERIOR CERVICAL PLATE SYSTEM THEKEN SPINE LLC
K080790 03/20/2008 MODIFICATION TO THEKEN ATOLL CERVICO-THORACIC SYSTEM THEKEN SPINE LLC
K070786 03/22/2007 X-POD ADJUSTABLE VERTEBRAL BODY REPLACEMENT THEKEN SPINE LLC
K080822 03/24/2008 VU APOD INTERVERTABRAL BODY FUSION DEVICE THEKEN SPINE LLC
K070962 04/05/2007 CORAL PEDICLE SCREW SYSTEM THEKEN SPINE LLC
K100970 04/08/2010 STAINLESS STEEL SPINAL SYSTEM THEKEN SPINE LLC
K071031 04/11/2007 VU E*POD VERTEBRAL BODY REPLACEMENT THEKEN SPINE LLC
K091266 04/30/2009 THEKEN CORAL SPINAL SYSTEM THEKEN SPINE LLC
K121482 05/18/2012 INSTRUMENT SYSTEM FOR ENDOSCOPIC SPINAL SURGERY THEKEN SPINE LLC
K081414 05/20/2008 MODIFICATION TO CORAL SPINAL SYSTEM THEKEN SPINE LLC
K111675 06/15/2011 VU C*POD INTERVERTEBRAL BODY FUSION DEVICE THEKEN SPINE LLC
K102323 08/17/2010 CERVICAL STANDALONE INTERVERTEBRAL BODY FUSION DEVICE THEKEN SPINE LLC
K072407 08/27/2007 BODYFORM THORACIC FIXATION SYSTEM THEKEN SPINE LLC
K082712 09/16/2008 THEKEN SPINE VU EPOD AND VU LPOD SYSTEM THEKEN SPINE LLC
K083073 10/15/2008 THEKEN ATOLL CERVICO-THORACIC SYSTEM THEKEN SPINE LLC
K103228 11/02/2010 PARAMOUNT R IBF DEVICE THEKEN SPINE LLC
K083863 12/29/2008 THEKEN ATOLL OCT SPINAL SYSTEM THEKEN SPINE LLC
K101310 05/11/2010 VU APOD INTERVERTEBRAL BODY FUSION DEVICE THEKEN SPINE LLC


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