This medical device record is a pma supplement. A supplement may have changed the device description/function or indication from that approved in the original pma. Be sure to look at the original pma record for more information.
Approval for the inclusion of additional fusion cage component designs for use with the infuse bone graft component. The following part numbers were not included as part of this request: 890226, 890229, 890243, 890246, 890249, 9012426 and 9012429; the device, as modified, will be marketed under the following trade names: infuse bone graft/lt-cage lumbar tapered fusion device; infuse bone graft/inter fix threaded fusion device; and infuse bone graft/inter fix rp threaded fusion device. For purposes of clarity, the lt-cage lumbar tapered fusion device, inter fix threaded fusion devcie, and inter fix rp threaded fusion device components are collectively referred to as "interbody fusion device" for the remainder of this approval order. The device is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (ddd) at one level from l4-s1. Ddd is defined as discogenic back pain with degeneration of the disc confirmed by patient history, function deficit and/or neurological deficit and radiographic studies. These ddd patients may also have up to grade i spondylolisthesis at the involved level. The infuse bone graft/lt-cage devices are to be implanted via an anterior open or a laparoscopic approach. The infuse bone graft/inter fix threaded fusion device; and infuse bone graft/inter fix rp threaded fusion device are to be implanted via an anterior open approach only. Patients receiving the infuse bone graft/interbody fusion device should have had at least six months of nonoperative treatment prior to treatment with the infuse bone graft/interbody fusion device.
| Device | INFUSE BONE GRAFT/LT-CAGE LUMBAR TAPERED FUSION DEVICE |
| Classification Name | Filler, Recombinant Human Bone Morphogenetic Protein, Collagen Scaffold With Metal Prosthesis, Osteoinduction |
| Generic Name | Filler, Recombinant Human Bone Morphogenetic Protein, Collagen Scaffold With Metal Prosthesis, Osteoinduction |
| Applicant | Medtronic Sofamor Danek USA, Inc. |
| Date Received | 2003-07-01 |
| Decision Date | 2003-12-01 |
| PMA | P000058 |
| Supplement | S004 |
| Product Code | NEK |
| Advisory Committee | Orthopedic |
| Supplement Type | Normal 180 Day Track |
| Supplement Reason | Change Design/components/specifications/material |
| Expedited Review | No |
| Combination Product | Yes |
| Applicant Address | Medtronic Sofamor Danek USA, Inc. 1800 Pyramid Place memphis, TN 38132 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P000058 | Original Filing | |
| S087 | 2022-07-21 | 30-day Notice |
| S086 | 2022-05-10 | 30-day Notice |
| S085 | 2022-01-20 | 30-day Notice |
| S084 | 2021-03-09 | 30-day Notice |
| S083 | 2021-01-15 | 30-day Notice |
| S082 | 2020-07-30 | 30-day Notice |
| S081 | ||
| S080 | ||
| S079 | ||
| S078 | 2020-06-11 | 30-day Notice |
| S077 | 2019-11-04 | 30-day Notice |
| S076 | 2019-10-31 | 30-day Notice |
| S075 | 2019-09-25 | 30-day Notice |
| S074 | ||
| S073 | ||
| S072 | 2019-06-28 | 30-day Notice |
| S071 | 2018-10-17 | Normal 180 Day Track |
| S070 | 2018-10-02 | 30-day Notice |
| S069 | 2018-08-02 | 30-day Notice |
| S068 | 2017-11-13 | 30-day Notice |
| S067 | 2017-05-23 | 30-day Notice |
| S066 | ||
| S065 | 2017-04-28 | Normal 180 Day Track |
| S064 | 2017-02-03 | 30-day Notice |
| S063 | 2017-01-23 | 30-day Notice |
| S062 | 2016-08-31 | 30-day Notice |
| S061 | 2016-07-11 | 30-day Notice |
| S060 | 2016-06-21 | Normal 180 Day Track |
| S059 | 2015-04-13 | Normal 180 Day Track |
| S058 | 2014-10-29 | Real-time Process |
| S057 | 2014-10-27 | Normal 180 Day Track No User Fee |
| S056 | 2014-01-27 | Normal 180 Day Track |
| S055 | ||
| S054 | 2013-10-25 | Real-time Process |
| S053 | 2013-02-26 | 30-day Notice |
| S052 | 2013-01-14 | 30-day Notice |
| S051 | 2012-12-21 | 30-day Notice |
| S050 | 2012-08-21 | 135 Review Track For 30-day Notice |
| S049 | 2011-12-19 | Normal 180 Day Track |
| S048 | 2011-10-20 | Special (immediate Track) |
| S047 | 2011-10-04 | 135 Review Track For 30-day Notice |
| S046 | 2011-08-26 | Real-time Process |
| S045 | 2011-08-19 | Special (immediate Track) |
| S044 | 2011-06-16 | 135 Review Track For 30-day Notice |
| S043 | 2011-02-15 | 135 Review Track For 30-day Notice |
| S042 | 2011-01-13 | 30-day Notice |
| S041 | 2010-09-30 | 135 Review Track For 30-day Notice |
| S040 | 2010-09-30 | 135 Review Track For 30-day Notice |
| S039 | 2010-09-01 | Normal 180 Day Track No User Fee |
| S038 | 2010-06-03 | 135 Review Track For 30-day Notice |
| S037 | 2010-05-14 | Normal 180 Day Track No User Fee |
| S036 | 2010-02-24 | Special (immediate Track) |
| S035 | ||
| S034 | 2009-09-01 | 135 Review Track For 30-day Notice |
| S033 | 2009-03-25 | 135 Review Track For 30-day Notice |
| S032 | 2009-03-16 | Special (immediate Track) |
| S031 | 2008-12-23 | Real-time Process |
| S030 | 2008-11-21 | 135 Review Track For 30-day Notice |
| S029 | 2008-08-29 | 135 Review Track For 30-day Notice |
| S028 | 2008-01-14 | 135 Review Track For 30-day Notice |
| S027 | 2007-11-16 | Normal 180 Day Track No User Fee |
| S026 | 2007-11-06 | Normal 180 Day Track No User Fee |
| S025 | 2007-07-31 | 135 Review Track For 30-day Notice |
| S024 | ||
| S023 | 2007-04-06 | 135 Review Track For 30-day Notice |
| S022 | 2007-03-05 | Normal 180 Day Track |
| S021 | 2006-12-22 | 135 Review Track For 30-day Notice |
| S020 | 2006-10-27 | Normal 180 Day Track |
| S019 | 2006-10-12 | Special (immediate Track) |
| S018 | ||
| S017 | 2005-02-22 | Real-time Process |
| S016 | 2005-02-04 | 135 Review Track For 30-day Notice |
| S015 | 2004-11-15 | Real-time Process |
| S014 | 2004-09-17 | 135 Review Track For 30-day Notice |
| S013 | ||
| S012 | ||
| S011 | ||
| S010 | 2004-05-20 | Real-time Process |
| S009 | 2004-04-20 | Real-time Process |
| S008 | 2004-03-19 | Special (immediate Track) |
| S007 | 2004-03-04 | Special (immediate Track) |
| S006 | 2003-08-26 | Normal 180 Day Track No User Fee |
| S005 | 2003-08-22 | Normal 180 Day Track No User Fee |
| S004 | 2003-07-01 | Normal 180 Day Track |
| S003 | 2002-12-16 | Normal 180 Day Track |
| S002 | ||
| S001 |