Other products from "L&K BIOMED CO. ,LTD."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 08809649611958 6614-1765S CastleLoc-P Anterior Cervical Plate (4Level-Neat Type) 65mm 1EA KWQ Appliance, Fixation, Spinal Intervertebral Body 2 CastleLoc-P Anterior Cervical Plate System
2 08806344397149 1043-0054 Crosslink 50-70mm KWQ,KWP,NKB Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Inte Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal,Thoracolumbosacral Pedicle Screw System 2 LnK/OpenLoc-L Spinal Fixation System
3 08806344394636 2631-5545S 2631-5545S NKB Thoracolumbosacral Pedicle Screw System 2 LnK/PathLoc-L MIS Spinal System
4 08806344377844 3953-2512 3953-2512 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 LnK Lumbar Interbody Fusion Cage System/PathLoc-LC Lateral Cage System
5 08806344363335 1022-1030S Arch Screw Open Type 30mm OUR Sacroiliac Joint Fixation 2 PathLoc-SI Joint Fusion System
6 08806344337350 1023-6050 1023-6050 Locking Screw Ø 6.0 50mm OUR Sacroiliac Joint Fixation 2 PathLoc-SI Joint Fusion System
7 08806344347861 1313-6040 Mono Axial Screw Ø6.0, 40mm NKB,KWP,KWQ Thoracolumbosacral Pedicle Screw System,Appliance, Fixation, Spinal Interlaminal Thoracolumbosacral Pedicle Screw System,Appliance, Fixation, Spinal Interlaminal,Appliance, Fixation, Spinal Intervertebral Body 2 OpenLoc-L Spinal Fixation System
8 08806189892878 5108-1515S L&K Biomed ACIF PEEK Cage (STERILE)15*15*08mm 1EA ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 LnK Cervical Interbody Fusion Cage System
9 08806344320338 1611-1408 1611-1408 Ramped Hook, Narrow, 8mm NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 LnK Spinal Fixation System
10 08806189893424 6711-1727 CastleLoc-P Anterior Cervical Plate (1Level-Contour Type) 27mm 1EA KWQ Appliance, Fixation, Spinal Intervertebral Body 2 CastleLoc-P Anterior Cervical Plate System
11 08806189893394 6711-1721 CastleLoc-P Anterior Cervical Plate (1Level-Contour Type) 21mm 1EA KWQ Appliance, Fixation, Spinal Intervertebral Body 2 CastleLoc-P Anterior Cervical Plate System
12 08806189896227 5207-1217 L&K Biomed ACIF PEEK Cage 12*17*07mm 7° 1EA ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 LnK Cervical Interbody Fusion Cage System
13 08806189872320 2526-6095 2526-6095 L&K Biomed MIS Rod, Cuved 6.0x95mm 1EA NKB,MNI,MNH Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation 2 LnK MIS Spinal System
14 08806189861652 1088-6360 L&K Biomed Rod, Curved, Double Stopper, CoCrMo 6.35x60mm 1EA NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 LnK Spinal Fixation System
15 08806189822844 1422-8030 1422-8030 L&K Biomed Poly Axial Screw 8.0x30mm 1EA KWP,MNI,MNH,KWQ,NKB Appliance, Fixation, Spinal Interlaminal,Orthosis, Spinal Pedicle Fixation,Ortho Appliance, Fixation, Spinal Interlaminal,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease 2 LnK Spinal Fixation System
16 08806189822837 1422-8025 1422-8025 L&K Biomed Poly Axial Screw 8.0x25mm 1EA NKB,KWQ,MNH,MNI,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Appliance, Fixa Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Appliance, Fixation, Spinal Intervertebral Body,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Appliance, Fixation, Spinal Interlaminal 2 LnK Spinal Fixation System
17 08806189854517 1054-5055 1054-5055 L&K Biomed Rod, Curved, Titanium 5.0x55mm 1EA NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 LnK Spinal Fixation System
18 08806189848493 1081-63460 L&K Biomed Rod, Straight, Stopper, CoCrMo 6.35x460mm 1EA NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 LnK Spinal Fixation System
19 08806189845676 1061-63560 L&K Biomed Rod, Straight, Stopper, Titanium 6.0x560mm 1EA MNI,NKB,KWP,KWQ,MNH Orthosis, Spinal Pedicle Fixation,Orthosis, Spinal Pedicle Fixation, For Degener Orthosis, Spinal Pedicle Fixation,Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Appliance, Fixation, Spinal Interlaminal,Appliance, Fixation, Spinal Intervertebral Body,Orthosis, Spondylolisthesis Spinal Fixation 2 LnK Spinal Fixation System
20 08806189845034 1061-6360 L&K Biomed Rod, Straight, Stopper, Titanium 6.0x60mm 1EA MNI,NKB,KWP,KWQ,MNH Orthosis, Spinal Pedicle Fixation,Orthosis, Spinal Pedicle Fixation, For Degener Orthosis, Spinal Pedicle Fixation,Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Appliance, Fixation, Spinal Interlaminal,Appliance, Fixation, Spinal Intervertebral Body,Orthosis, Spondylolisthesis Spinal Fixation 2 LnK Spinal Fixation System
21 08806189822035 1422-6530 1422-6530 L&K Biomed Poly Axial Screw 6.5x30mm 1EA NKB,KWQ,MNH,MNI,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Appliance, Fixa Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Appliance, Fixation, Spinal Intervertebral Body,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Appliance, Fixation, Spinal Interlaminal 2 LnK Spinal Fixation System
22 08800108646825 6114-5028 Cervical Poly Axial Screw – screw neck Ø 3.0 5x28mm NKG,KWP Posterior Cervical Screw System,Appliance, Fixation, Spinal Interlaminal 2 LnK/CastleLoc-S Posterior Cervical Fixation System
23 08806189836919 1071-63560 L&K Biomed Rod, Straight, CoCrMo 6.0x560mm 1EA NKB,KWQ,MNH,MNI,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Appliance, Fixa Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Appliance, Fixation, Spinal Intervertebral Body,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Appliance, Fixation, Spinal Interlaminal 2 LnK Spinal Fixation System
24 08806189836612 1071-63260 L&K Biomed Rod, Straight, CoCrMo 6.0x260mm 1EA MNI,NKB,KWP,KWQ,MNH Orthosis, Spinal Pedicle Fixation,Orthosis, Spinal Pedicle Fixation, For Degener Orthosis, Spinal Pedicle Fixation,Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Appliance, Fixation, Spinal Interlaminal,Appliance, Fixation, Spinal Intervertebral Body,Orthosis, Spondylolisthesis Spinal Fixation 2 LnK Spinal Fixation System
25 08806189835783 1071-60180 L&K Biomed Rod, Straight, CoCrMo 6.0x180mm 1EA KWP,KWQ,NKB Appliance, Fixation, Spinal Interlaminal,Appliance, Fixation, Spinal Interverteb Appliance, Fixation, Spinal Interlaminal,Appliance, Fixation, Spinal Intervertebral Body,Thoracolumbosacral Pedicle Screw System 2 LnK Spinal Fixation System
26 08806189835332 1071-55440 L&K Biomed Rod, Straight, CoCrMo 6.0x440mm 1EA KWP,KWQ,NKB Appliance, Fixation, Spinal Interlaminal,Appliance, Fixation, Spinal Interverteb Appliance, Fixation, Spinal Interlaminal,Appliance, Fixation, Spinal Intervertebral Body,Thoracolumbosacral Pedicle Screw System 2 LnK Spinal Fixation System
27 08800108646689 6114-4542 Cervical Poly Axial Screw – screw neck Ø 3.0 4.5x42mm NKG,KWP Posterior Cervical Screw System,Appliance, Fixation, Spinal Interlaminal 2 LnK/CastleLoc-S Posterior Cervical Fixation System
28 08800108646658 6114-4536 Cervical Poly Axial Screw – screw neck Ø 3.0 4.5x36mm NKG,KWP Posterior Cervical Screw System,Appliance, Fixation, Spinal Interlaminal 2 LnK/CastleLoc-S Posterior Cervical Fixation System
29 08806189827320 1352-8555 1352-8555 L&K Biomed Reduction Poly Axial Screw 8.5x55mm 1EA MNI,MNH,KWQ,KWP,NKB Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Ap Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal,Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease 2 LnK Spinal Fixation System
30 08800108646603 6114-4526 Cervical Poly Axial Screw – screw neck Ø 3.0 4.5x26mm NKG,KWP Posterior Cervical Screw System,Appliance, Fixation, Spinal Interlaminal 2 LnK/CastleLoc-S Posterior Cervical Fixation System
31 08800108646573 6114-4520 Cervical Poly Axial Screw – screw neck Ø 3.0 4.5x20mm NKG,KWP Posterior Cervical Screw System,Appliance, Fixation, Spinal Interlaminal 2 LnK/CastleLoc-S Posterior Cervical Fixation System
32 08800108646542 6114-4514 Cervical Poly Axial Screw – screw neck Ø 3.0 4.5x14mm NKG,KWP Posterior Cervical Screw System,Appliance, Fixation, Spinal Interlaminal 2 LnK/CastleLoc-S Posterior Cervical Fixation System
33 08800108646351 6111-5518 Cervical Poly Axial Screw – screw neck Ø 2.4 5.5x18mm NKG,KWP Posterior Cervical Screw System,Appliance, Fixation, Spinal Interlaminal 2 LnK/CastleLoc-S Posterior Cervical Fixation System
34 08806189813880 1432-4060 1432-4060 L&K Biomed Reductionn Mono Axial Screw 4.0x60mm 1EA MNI,KWP,KWQ,NKB,MNH Orthosis, Spinal Pedicle Fixation,Appliance, Fixation, Spinal Interlaminal,Appli Orthosis, Spinal Pedicle Fixation,Appliance, Fixation, Spinal Interlaminal,Appliance, Fixation, Spinal Intervertebral Body,Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spondylolisthesis Spinal Fixation 2 LnK Spinal Fixation System
35 08800061383850 1074-55115S Curved Rod(Standard) Ø5.5 , 115mm NKB,KWP,KWQ Thoracolumbosacral Pedicle Screw System,Appliance, Fixation, Spinal Interlaminal Thoracolumbosacral Pedicle Screw System,Appliance, Fixation, Spinal Interlaminal,Appliance, Fixation, Spinal Intervertebral Body 2 AccelFix Spinal Fixation System
36 08800108646221 6111-5034 Cervical Poly Axial Screw – screw neck Ø 2.4 5x34mm NKG,KWP Posterior Cervical Screw System,Appliance, Fixation, Spinal Interlaminal 2 LnK/CastleLoc-S Posterior Cervical Fixation System
37 08800108646184 6111-5026 Cervical Poly Axial Screw – screw neck Ø 2.4 5x26mm NKG,KWP Posterior Cervical Screw System,Appliance, Fixation, Spinal Interlaminal 2 LnK/CastleLoc-S Posterior Cervical Fixation System
38 08800108646153 6111-5020 Cervical Poly Axial Screw – screw neck Ø 2.4 5x20mm NKG,KWP Posterior Cervical Screw System,Appliance, Fixation, Spinal Interlaminal 2 LnK/CastleLoc-S Posterior Cervical Fixation System
39 08806189804222 1312-85145 1312-85145 NKB,MNH,KWQ,KWP,MNI Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spond Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal,Orthosis, Spinal Pedicle Fixation 2 LnK Spinal Fixation System
40 08800061391657 1043-0054S Crosslink 50-70mm NKB,KWP,KWQ Thoracolumbosacral Pedicle Screw System,Appliance, Fixation, Spinal Interlaminal Thoracolumbosacral Pedicle Screw System,Appliance, Fixation, Spinal Interlaminal,Appliance, Fixation, Spinal Intervertebral Body 2 AccelFix Spinal Fixation System
41 08800061391640 1043-0048S Crosslink 40-53mm NKB,KWP,KWQ Thoracolumbosacral Pedicle Screw System,Appliance, Fixation, Spinal Interlaminal Thoracolumbosacral Pedicle Screw System,Appliance, Fixation, Spinal Interlaminal,Appliance, Fixation, Spinal Intervertebral Body 2 AccelFix Spinal Fixation System
42 08800061391633 1043-0042S Crosslink 34-42mm NKB,KWP,KWQ Thoracolumbosacral Pedicle Screw System,Appliance, Fixation, Spinal Interlaminal Thoracolumbosacral Pedicle Screw System,Appliance, Fixation, Spinal Interlaminal,Appliance, Fixation, Spinal Intervertebral Body 2 AccelFix Spinal Fixation System
43 08800061391626 1043-0034S Crosslink 30-34mm NKB,KWP,KWQ Thoracolumbosacral Pedicle Screw System,Appliance, Fixation, Spinal Interlaminal Thoracolumbosacral Pedicle Screw System,Appliance, Fixation, Spinal Interlaminal,Appliance, Fixation, Spinal Intervertebral Body 2 AccelFix Spinal Fixation System
44 08800061390605 2512-5580S MIS Curved Rod Ø5.5 , 80mm NKB,KWP,KWQ Thoracolumbosacral Pedicle Screw System,Appliance, Fixation, Spinal Interlaminal Thoracolumbosacral Pedicle Screw System,Appliance, Fixation, Spinal Interlaminal,Appliance, Fixation, Spinal Intervertebral Body 2 AccelFix Spinal Fixation System
45 08800061390599 2512-5575S MIS Curved Rod Ø5.5 , 75mm NKB,KWP,KWQ Thoracolumbosacral Pedicle Screw System,Appliance, Fixation, Spinal Interlaminal Thoracolumbosacral Pedicle Screw System,Appliance, Fixation, Spinal Interlaminal,Appliance, Fixation, Spinal Intervertebral Body 2 AccelFix Spinal Fixation System
46 08800061390582 2512-5570S MIS Curved Rod Ø5.5 , 70mm NKB,KWP,KWQ Thoracolumbosacral Pedicle Screw System,Appliance, Fixation, Spinal Interlaminal Thoracolumbosacral Pedicle Screw System,Appliance, Fixation, Spinal Interlaminal,Appliance, Fixation, Spinal Intervertebral Body 2 AccelFix Spinal Fixation System
47 08800061390575 2512-5565S MIS Curved Rod Ø5.5 , 65mm NKB,KWP,KWQ Thoracolumbosacral Pedicle Screw System,Appliance, Fixation, Spinal Interlaminal Thoracolumbosacral Pedicle Screw System,Appliance, Fixation, Spinal Interlaminal,Appliance, Fixation, Spinal Intervertebral Body 2 AccelFix Spinal Fixation System
48 08800061390568 2512-5560S MIS Curved Rod Ø5.5 , 60mm NKB,KWP,KWQ Thoracolumbosacral Pedicle Screw System,Appliance, Fixation, Spinal Interlaminal Thoracolumbosacral Pedicle Screw System,Appliance, Fixation, Spinal Interlaminal,Appliance, Fixation, Spinal Intervertebral Body 2 AccelFix Spinal Fixation System
49 08800061390551 2512-5555S MIS Curved Rod Ø5.5 , 55mm NKB,KWP,KWQ Thoracolumbosacral Pedicle Screw System,Appliance, Fixation, Spinal Interlaminal Thoracolumbosacral Pedicle Screw System,Appliance, Fixation, Spinal Interlaminal,Appliance, Fixation, Spinal Intervertebral Body 2 AccelFix Spinal Fixation System
50 08800061390544 2512-5550S MIS Curved Rod Ø5.5 , 50mm NKB,KWP,KWQ Thoracolumbosacral Pedicle Screw System,Appliance, Fixation, Spinal Interlaminal Thoracolumbosacral Pedicle Screw System,Appliance, Fixation, Spinal Interlaminal,Appliance, Fixation, Spinal Intervertebral Body 2 AccelFix Spinal Fixation System
Other products with the same Product Code "MAX"
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.