Other products from "ICOTEC AG"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 07640164848365 13-59-42513 13-59-42513 icotec Lumbar Cage PLIF 4° / 25 mm x 13 mm MAX,ODP Intervertebral Fusion Device With Bone Graft, Lumbar,Intervertebral Fusion Devic Intervertebral Fusion Device With Bone Graft, Lumbar,Intervertebral Fusion Device With Bone Graft, Cervical 2 icotec Lumbar Cage PLIF 4° / 25 mm x 13 mm
2 07640140438436 12-74-18-86 icotec Ant. Cervical Plate, 4 Segmental, 86 mm KWQ Appliance, Fixation, Spinal Intervertebral Body 2 icotec Ant. Cervical Plate, 4 Segmental, 86 mm
3 07640164844824 16-6022-57550 VADER Pedicle System 6.0, Screw, Carbon/PEEK, Polyax., Fen., Ø 7.5 x 50 mm NKB,PML Thoracolumbosacral Pedicle Screw System,Bone Cement, Posterior Screw Augmentation 2 VADER Pedicle System 6.0, Screw, Carbon/PEEK, Polyax., Fen., Ø 7.5 x 50 mm
4 07640164842196 42-735 42-735 VADER Pedicle System, French Rod Bender NKB Thoracolumbosacral Pedicle Screw System 2 VADER Pedicle System, French Rod Bender
5 07640172552131 42-703 42-703 VADER Pedicle System, Torque Wrench (Push-Mechanism), Hudson Coupling, 12Nm NKB Thoracolumbosacral Pedicle Screw System 2 VADER Pedicle System, Torque Wrench (Push-Mechanism), Hudson Coupling, 12Nm
6 07640172552117 42-733 42-733 VADER Pedicle System, T-Handle, Ratchet (Push-Mechanism), 1/4" Coupling NKB Thoracolumbosacral Pedicle Screw System 2 VADER Pedicle System, T-Handle, Ratchet (Push-Mechanism), 1/4" Coupling
7 07640172551356 44-005-75 44-005-75 KONG-TL VBR System, Trial Implant, XL + EM, Ø 19 mm x 75 mm MQP,PLR Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Devic Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Device - Cervical 2 KONG-TL VBR System, Trial Implant, XL + EM, Ø 19 mm x 75 mm
8 07640172551318 44-075 44-075 KONG-TL VBR System, Extension Rod MQP,PLR Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Devic Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Device - Cervical 2 KONG-TL VBR System, Extension Rod
9 07640172551233 42-862-1 42-862-1 icotec Instrument, Pedicle System MIS 2/2, Container Base NKB Thoracolumbosacral Pedicle Screw System 2 icotec Instrument, Pedicle System MIS 2/2, Container Base
10 07640172551127 44-040-03 44-040-03 KONG-TL VBR System, Impact Cap MQP,PLR Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Devic Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Device - Cervical 2 KONG-TL VBR System, Impact Cap
11 07640172550960 43-146 43-146 KONG-C VBR System, Trial End Plate, 6° / 14 x 13 mm MQP,PLR Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Devic Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Device - Cervical 2 KONG-C VBR System, Trial End Plate, 6° / 14 x 13 mm
12 07640172550939 43-090-1 43-090-1 KONG-C VBR System, KONG-C VBR M, Container Base MQP,PLR Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Devic Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Device - Cervical 2 KONG-C VBR System, KONG-C VBR M, Container Base
13 07640172550922 43-266 43-266 KONG-C VBR System, Trial Body, 66 mm MQP,PLR Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Devic Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Device - Cervical 2 KONG-C VBR System, Trial Body, 66 mm
14 07640172550915 43-264 43-264 KONG-C VBR System, Trial Body, 64 mm MQP,PLR Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Devic Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Device - Cervical 2 KONG-C VBR System, Trial Body, 64 mm
15 07640172550878 43-256 43-256 KONG-C VBR System, Trial Body, 56 mm MQP,PLR Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Devic Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Device - Cervical 2 KONG-C VBR System, Trial Body, 56 mm
16 07640172550823 43-246 43-246 KONG-C VBR System, Trial Body, 46 mm MQP,PLR Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Devic Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Device - Cervical 2 KONG-C VBR System, Trial Body, 46 mm
17 07640172550762 43-234 43-234 KONG-C VBR System, Trial Body, 34 mm MQO,PLR Prosthetic Disc Nucleus Device,Spinal Vertebral Body Replacement Device - Cervical 2 KONG-C VBR System, Trial Body, 34 mm
18 07640172550687 43-218 43-218 KONG-C VBR System, Trial Body, 18 mm MQP,PLR Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Devic Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Device - Cervical 2 KONG-C VBR System, Trial Body, 18 mm
19 07640164849898 12-80-1358-0 12-80-1358-0 KONG-C VBR M, Body, 58 mm MQP,PLR Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Devic Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Device - Cervical 2 KONG-C VBR M, Body, 58 mm
20 07640164849805 12-80-1340-0 12-80-1340-0 KONG-C VBR M, Body, 40 mm MQP,PLR Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Devic Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Device - Cervical 2 KONG-C VBR M, Body, 40 mm
21 07640164849799 12-80-1338-0 12-80-1338-0 KONG-C VBR M, Body, 38 mm MQP,PLR Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Devic Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Device - Cervical 2 KONG-C VBR M, Body, 38 mm
22 07640164849782 12-80-1336-0 12-80-1336-0 KONG-C VBR M, Body, 36 mm MQP,PLR Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Devic Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Device - Cervical 2 KONG-C VBR M, Body, 36 mm
23 07640164849751 12-80-1330-0 12-80-1330-0 KONG-C VBR M, Body, 30 mm MQP,PLR Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Devic Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Device - Cervical 2 KONG-C VBR M, Body, 30 mm
24 07640164848679 16-60-91205 icotec Pedicle System 6.0, Rod, Ti, Curved, Ø 6.0 r120 x 050 mm NKB Thoracolumbosacral Pedicle Screw System 2 icotec Pedicle System 6.0, Rod, Ti, Curved, Ø 6.0 r120 x 050 mm
25 07640164849607 16-6022-98550 icotec Pedicle System 6.0, Screw, Ti, Polyax., Fen., Ø 8.5 x 50 mm PML,NKB Bone Cement, Posterior Screw Augmentation,Thoracolumbosacral Pedicle Screw System 2 icotec Pedicle System 6.0, Screw, Ti, Polyax., Fen., Ø 8.5 x 50 mm
26 07640164849454 16-6024-56560 16-6024-56560 LightMore Pedicle System 6.0, Screw, Carbon/PEEK, Polyax., Noncann., Ø 6.5 x 60 mm NKB Thoracolumbosacral Pedicle Screw System 2 LightMore Pedicle System 6.0, Screw, Carbon/PEEK, Polyax., Noncann., Ø 6.5 x 60
27 07640164849409 16-6024-56535 16-6024-56535 LightMore Pedicle System 6.0, Screw, Carbon/PEEK, Polyax., Noncann., Ø 6.5 x 35 mm NKB Thoracolumbosacral Pedicle Screw System 2 LightMore Pedicle System 6.0, Screw, Carbon/PEEK, Polyax., Noncann., Ø 6.5 x 35
28 07640164849362 16-6024-55550 16-6024-55550 LightMore Pedicle System 6.0, Screw, Carbon/PEEK, Polyax., Noncann., Ø 5.5 x 50 mm NKB Thoracolumbosacral Pedicle Screw System 2 LightMore Pedicle System 6.0, Screw, Carbon/PEEK, Polyax., Noncann., Ø 5.5 x 50
29 07640164849294 16-6023-57555 16-6023-57555 VADERone Pedicle System, Screw, Carbon/PEEK, Polyaxial, Ø 7.5 x 55 mm NKB Thoracolumbosacral Pedicle Screw System 2 VADERone Pedicle System, Screw, Carbon/PEEK, Polyaxial, Ø 7.5 x 55 mm
30 07640164849232 16-6023-56560 16-6023-56560 VADERone Pedicle System, Screw, Carbon/PEEK, Polyaxial, Ø 6.5 x 60 mm NKB Thoracolumbosacral Pedicle Screw System 2 VADERone Pedicle System, Screw, Carbon/PEEK, Polyaxial, Ø 6.5 x 60 mm
31 07640164849218 16-6023-56550 16-6023-56550 VADERone Pedicle System, Screw, Carbon/PEEK, Polyaxial, Ø 6.5 x 50 mm NKB Thoracolumbosacral Pedicle Screw System 2 VADERone Pedicle System, Screw, Carbon/PEEK, Polyaxial, Ø 6.5 x 50 mm
32 07640164849195 16-6023-56540 16-6023-56540 VADERone Pedicle System, Screw, Carbon/PEEK, Polyaxial, Ø 6.5 x 40 mm NKB Thoracolumbosacral Pedicle Screw System 2 VADERone Pedicle System, Screw, Carbon/PEEK, Polyaxial, Ø 6.5 x 40 mm
33 07640164849157 16-6023-55555 16-6023-55555 VADERone Pedicle System, Screw, Carbon/PEEK, Polyaxial, Ø 5.5 x 55 mm NKB Thoracolumbosacral Pedicle Screw System 2 VADERone Pedicle System, Screw, Carbon/PEEK, Polyaxial, Ø 5.5 x 55 mm
34 07640164848341 13-59-42511 13-59-42511 icotec Lumbar Cage PLIF 4° / 25 mm x 11 mm MAX,ODP Intervertebral Fusion Device With Bone Graft, Lumbar,Intervertebral Fusion Devic Intervertebral Fusion Device With Bone Graft, Lumbar,Intervertebral Fusion Device With Bone Graft, Cervical 2 icotec Lumbar Cage PLIF 4° / 25 mm x 11 mm
35 07640164848716 16-60-91209 16-60-91209 icotec Pedicle System 6.0, Rod, Ti, Curved, Ø 6.0 r120 x 090 mm NKB Thoracolumbosacral Pedicle Screw System 2 icotec Pedicle System 6.0, Rod, Ti, Curved, Ø 6.0 r120 x 090 mm
36 07640164848532 16-60-90009 16-60-90009 icotec Pedicle System 6.0, Rod, Ti, Straight, Ø 6.0 r000 x 090 mm NKB Thoracolumbosacral Pedicle Screw System 2 icotec Pedicle System 6.0, Rod, Ti, Straight, Ø 6.0 r000 x 090 mm
37 07640164848464 42-825 42-825 VADER Pedicle System, Torque Increaser for Persuader Inline NKB,PML Thoracolumbosacral Pedicle Screw System,Bone Cement, Posterior Screw Augmentation 2 VADER Pedicle System, Torque Increaser for Persuader Inline
38 07640164848150 13-58-16-32-10-ITi 13-58-16-32-10-ITi icotec Lumbar Cage ETurn TLIF 10 x 16 mm MAX,ODP Intervertebral Fusion Device With Bone Graft, Lumbar,Intervertebral Fusion Devic Intervertebral Fusion Device With Bone Graft, Lumbar,Intervertebral Fusion Device With Bone Graft, Cervical 2 icotec Lumbar Cage ETurn TLIF 10 x 16 mm
39 07640164848136 13-58-16-32-08-ITi 13-58-16-32-08-ITi icotec Lumbar Cage ETurn TLIF 8 x 16 mm MAX,ODP Intervertebral Fusion Device With Bone Graft, Lumbar,Intervertebral Fusion Devic Intervertebral Fusion Device With Bone Graft, Lumbar,Intervertebral Fusion Device With Bone Graft, Cervical 2 icotec Lumbar Cage ETurn TLIF 8 x 16 mm
40 07640164848105 13-57-12-32-14-ITi 13-57-12-32-14-ITi icotec Lumbar Cage ETurn TLIF 14 x 12 mm MAX,ODP Intervertebral Fusion Device With Bone Graft, Lumbar,Intervertebral Fusion Devic Intervertebral Fusion Device With Bone Graft, Lumbar,Intervertebral Fusion Device With Bone Graft, Cervical 2 icotec Lumbar Cage ETurn TLIF 14 x 12 mm
41 07640164847993 13-41-0518 13-41-0518 icotec Cervical Cage Anatomic 5 x 18 mm MAX,ODP Intervertebral Fusion Device With Bone Graft, Lumbar,Intervertebral Fusion Devic Intervertebral Fusion Device With Bone Graft, Lumbar,Intervertebral Fusion Device With Bone Graft, Cervical 2 icotec Cervical Cage Anatomic 5 x 18 mm
42 07640164847924 13-41-0513 13-41-0513 icotec Cervical Cage Anatomic 5 x 13 mm MAX,ODP Intervertebral Fusion Device With Bone Graft, Lumbar,Intervertebral Fusion Devic Intervertebral Fusion Device With Bone Graft, Lumbar,Intervertebral Fusion Device With Bone Graft, Cervical 2 icotec Cervical Cage Anatomic 5 x 13 mm
43 07640164847740 44-000-00-33 44-000-00-33 KONG-TL VBR System, Trial End Plate, round, M , 0° x 33 mm MQP,PLR Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Devic Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Device - Cervical 2 KONG-TL VBR System, Trial End Plate, round, M , 0° x 33 mm
44 07640164847719 12-90-124320 12-90-124320 KONG-TL VBR, End Plate, rectangular, L and Screw, 12° x 43 mm MQP,PLR Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Devic Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Device - Cervical 2 KONG-TL VBR, End Plate, rectangular, L and Screw, 12° x 43 mm
45 07640164847641 12-90-043320 KONG-TL VBR, End Plate, rectangular, M and Screw, 4° x 33 mm MQP,PLR Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Devic Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Device - Cervical 2 KONG-TL VBR, End Plate, rectangular, M and Screw, 4° x 33 mm
46 07640164847610 12-90-003320 12-90-003320 KONG-TL VBR, End Plate, rectangular, M and Screw, 0° x 33 mm MQP,PLR Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Devic Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Device - Cervical 2 KONG-TL VBR, End Plate, rectangular, M and Screw, 0° x 33 mm
47 07640164847467 12-90-1920-0 12-90-1920-0 KONG-TL VBR, Extension, S and Screw, Ø 19 mm x 20 mm MQP,PLR Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Devic Spinal Vertebral Body Replacement Device,Spinal Vertebral Body Replacement Device - Cervical 2 KONG-TL VBR, Extension, S and Screw, Ø 19 mm x 20 mm
48 07640164847245 16-60-80035 16-60-80035 VADER Pedicle System MIS, Rod, Ti, Straight, Ø 6.0 r000 x 350 mm NKB,PML Thoracolumbosacral Pedicle Screw System,Bone Cement, Posterior Screw Augmentation 2 VADER Pedicle System MIS, Rod, Ti, Straight, Ø 6.0 r000 x 350 mm
49 07640164847115 16-60-80005 16-60-80005 VADER Pedicle System MIS, Rod, Ti, Straight, Ø 6.0 r000 x 50 mm NKB,PML Thoracolumbosacral Pedicle Screw System,Bone Cement, Posterior Screw Augmentation 2 VADER Pedicle System MIS, Rod, Ti, Straight, Ø 6.0 r000 x 50 mm
50 07640164847108 16-60-80004 16-60-80004 VADER Pedicle System MIS, Rod, Ti, Straight, Ø 6.0 r000 x 40 mm NKB,PML Thoracolumbosacral Pedicle Screw System,Bone Cement, Posterior Screw Augmentation 2 VADER Pedicle System MIS, Rod, Ti, Straight, Ø 6.0 r000 x 40 mm
Other products with the same Product Codes "MAX, ODP"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 08806378366258 1106-1655 1106-1655 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
2 08806378366241 1106-1455 1106-1455 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
3 08806378366234 1106-1255 1106-1255 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
4 08806378366227 1106-1055 1106-1055 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
5 08806378366210 1106-0855 1106-0855 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
6 08806378366203 1106-1650 1106-1650 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
7 08806378366197 1106-1450 1106-1450 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
8 08806378366180 1106-1250 1106-1250 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
9 08806378366173 1106-1050 1106-1050 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
10 08806378366166 1106-0850 1106-0850 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
11 08806378366159 1106-1645 1106-1645 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
12 08806378366142 1106-1445 1106-1445 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
13 08806378366135 1106-1245 1106-1245 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
14 08806378366128 1106-1045 1106-1045 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
15 08806378366111 1106-0845 1106-0845 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
16 08806378366104 1106-1640 1106-1640 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
17 08806378366098 1106-1440 1106-1440 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
18 08806378366081 1106-1240 1106-1240 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
19 08806378366074 1106-1040 1106-1040 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
20 08806378366067 1106-0840 1106-0840 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
21 08806378366050 1105-1655 1105-1655 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
22 08806378366043 1105-1455 1105-1455 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
23 08806378366036 1105-1255 1105-1255 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
24 08806378366029 1105-1055 1105-1055 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
25 08806378366012 1105-0855 1105-0855 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
26 08806378366005 1105-1650 1105-1650 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
27 08806378365992 1105-1450 1105-1450 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
28 08806378365985 1105-1250 1105-1250 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
29 08806378365978 1105-1050 1105-1050 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
30 08806378365961 1105-0850 1105-0850 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
31 08806378365954 1105-1645 1105-1645 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
32 08806378365947 1105-1445 1105-1445 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
33 08806378365930 1105-1245 1105-1245 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
34 08806378365923 1105-1045 1105-1045 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
35 08806378365916 1105-0845 1105-0845 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
36 08806378365909 1105-1640 1105-1640 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
37 08806378365893 1105-1440 1105-1440 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
38 08806378365886 1105-1240 1105-1240 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
39 08806378365879 1105-1040 1105-1040 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
40 08806378365862 1105-0840 1105-0840 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cages GS MEDICAL CO., LTD.
41 08806378362854 1104-0716 1104-0716 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Cages GS MEDICAL CO., LTD.
42 08806378362847 1104-0715 1104-0715 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Cages GS MEDICAL CO., LTD.
43 08806378362830 1104-0714 1104-0714 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Cages GS MEDICAL CO., LTD.
44 08806378362823 1104-0713 1104-0713 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Cages GS MEDICAL CO., LTD.
45 08806378362816 1104-0712 1104-0712 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Cages GS MEDICAL CO., LTD.
46 08806378362809 1104-0711 1104-0711 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Cages GS MEDICAL CO., LTD.
47 08806378362793 1104-0710 1104-0710 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Cages GS MEDICAL CO., LTD.
48 08806378362786 1104-0709 1104-0709 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Cages GS MEDICAL CO., LTD.
49 08806378362779 1104-0708 1104-0708 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Cages GS MEDICAL CO., LTD.
50 08806378362762 1104-0707 1104-0707 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Cages GS MEDICAL CO., LTD.