| No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
|---|---|---|---|---|---|---|---|---|
| 1 | 10888857557291 | PRO-1216 | PRO-1216 | Implant Removal Tool | LXH | Orthopedic manual surgical instrument | 1 | ALEUTIAN Interbody Systems |
| 2 | 10888857554764 | PRO-1241-02 | PRO-1241-02 | Disc Spreader | LXH | Orthopedic manual surgical instrument | 1 | ALEUTIAN Interbody Systems |
| 3 | 10888857554757 | PRO-1241-01 | PRO-1241-01 | Disc Spreader | LXH | Orthopedic manual surgical instrument | 1 | ALEUTIAN Interbody Systems |
| 4 | 10888857548770 | PRO-1161-02 | PRO-1161-02 | Inner Shaft | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | ALEUTIAN® Interbody Systems |
| 5 | 10888857548763 | PRO-1161-01 | PRO-1161-01 | Trial Inserter | MQP,ODP,MAX | Spinal vertebral body replacement device,Intervertebral fusion device with bone Spinal vertebral body replacement device,Intervertebral fusion device with bone graft, cervical,Intervertebral fusion device with bone graft, lumbar | 2 | ALEUTIAN® Interbody Systems |
| 6 | 10888857528260 | PRO-1109 | PRO-1109 | Trial Inserter Size 25° | ODP,MQP,MAX | Intervertebral fusion device with bone graft, cervical,Spinal vertebral body rep Intervertebral fusion device with bone graft, cervical,Spinal vertebral body replacement device,Intervertebral fusion device with bone graft, lumbar | 2 | ALEUTIAN® Interbody Systems |
| 7 | 10888857527966 | PRO-1107-02 | PRO-1107-02 | Threaded Connector | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | ALEUTIAN® Interbody Systems |
| 8 | 10888857522237 | SP-4214-99 | SP-4214-99 | Trial Size 13x16x6 mm, 12° | ODP,MQP,MAX | Intervertebral fusion device with bone graft, cervical,Spinal vertebral body rep Intervertebral fusion device with bone graft, cervical,Spinal vertebral body replacement device,Intervertebral fusion device with bone graft, lumbar | 2 | ALEUTIAN® Interbody Systems |
| 9 | 10888857522220 | SP-4214-98 | SP-4214-98 | Trial Size 13x16x15 mm, 7° | ODP,MQP,MAX | Intervertebral fusion device with bone graft, cervical,Spinal vertebral body rep Intervertebral fusion device with bone graft, cervical,Spinal vertebral body replacement device,Intervertebral fusion device with bone graft, lumbar | 2 | ALEUTIAN® Interbody Systems |
| 10 | 10888857522213 | SP-4214-97 | SP-4214-97 | Trial Size 13x16x14 mm, 7° | MQP,MAX,ODP | Spinal vertebral body replacement device,Intervertebral fusion device with bone Spinal vertebral body replacement device,Intervertebral fusion device with bone graft, lumbar,Intervertebral fusion device with bone graft, cervical | 2 | ALEUTIAN® Interbody Systems |
| 11 | 10888857522206 | SP-4214-96 | SP-4214-96 | Trial Size 13x16x13 mm, 7° | MQP,ODP,MAX | Spinal vertebral body replacement device,Intervertebral fusion device with bone Spinal vertebral body replacement device,Intervertebral fusion device with bone graft, cervical,Intervertebral fusion device with bone graft, lumbar | 2 | ALEUTIAN® Interbody Systems |
| 12 | 10888857522190 | SP-4214-95 | SP-4214-95 | Trial Size 13x16x12 mm, 7° | MAX,ODP,MQP | Intervertebral fusion device with bone graft, lumbar,Intervertebral fusion devic Intervertebral fusion device with bone graft, lumbar,Intervertebral fusion device with bone graft, cervical,Spinal vertebral body replacement device | 2 | ALEUTIAN® Interbody Systems |
| 13 | 10888857522183 | SP-4214-94 | SP-4214-94 | Trial Size 13x16x11 mm, 7° | MAX,MQP,ODP | Intervertebral fusion device with bone graft, lumbar,Spinal vertebral body repla Intervertebral fusion device with bone graft, lumbar,Spinal vertebral body replacement device,Intervertebral fusion device with bone graft, cervical | 2 | ALEUTIAN® Interbody Systems |
| 14 | 10888857522176 | SP-4214-93 | SP-4214-93 | Trial Size 13x16x10 mm, 7° | MQP,ODP,MAX | Spinal vertebral body replacement device,Intervertebral fusion device with bone Spinal vertebral body replacement device,Intervertebral fusion device with bone graft, cervical,Intervertebral fusion device with bone graft, lumbar | 2 | ALEUTIAN® Interbody Systems |
| 15 | 10888857522169 | SP-4214-92 | SP-4214-92 | Trial Size 13x16x9 mm, 7° | ODP,MQP,MAX | Intervertebral fusion device with bone graft, cervical,Spinal vertebral body rep Intervertebral fusion device with bone graft, cervical,Spinal vertebral body replacement device,Intervertebral fusion device with bone graft, lumbar | 2 | ALEUTIAN® Interbody Systems |
| 16 | 10888857522152 | SP-4214-91 | SP-4214-91 | Trial Size 13x16x8 mm, 7° | ODP,MAX,MQP | Intervertebral fusion device with bone graft, cervical,Intervertebral fusion dev Intervertebral fusion device with bone graft, cervical,Intervertebral fusion device with bone graft, lumbar,Spinal vertebral body replacement device | 2 | ALEUTIAN® Interbody Systems |
| 17 | 10888857522145 | SP-4214-90 | SP-4214-90 | Trial Size 13x16x7 mm, 7° | MQP,ODP,MAX | Spinal vertebral body replacement device,Intervertebral fusion device with bone Spinal vertebral body replacement device,Intervertebral fusion device with bone graft, cervical,Intervertebral fusion device with bone graft, lumbar | 2 | ALEUTIAN® Interbody Systems |
| 18 | 10888857522138 | SP-4214-89 | SP-4214-89 | Trial Size 13x16x6 mm, 7° | MQP,MAX,ODP | Spinal vertebral body replacement device,Intervertebral fusion device with bone Spinal vertebral body replacement device,Intervertebral fusion device with bone graft, lumbar,Intervertebral fusion device with bone graft, cervical | 2 | ALEUTIAN® Interbody Systems |
| 19 | 10888857522121 | SP-4214-88 | SP-4214-88 | Trial Size 13x16x5 mm, 7° | ODP,MQP,MAX | Intervertebral fusion device with bone graft, cervical,Spinal vertebral body rep Intervertebral fusion device with bone graft, cervical,Spinal vertebral body replacement device,Intervertebral fusion device with bone graft, lumbar | 2 | ALEUTIAN® Interbody Systems |
| 20 | 10888857522114 | SP-4214-87 | SP-4214-87 | Trial Size 13x16x15 mm, 0° | MAX,MQP,ODP | Intervertebral fusion device with bone graft, lumbar,Spinal vertebral body repla Intervertebral fusion device with bone graft, lumbar,Spinal vertebral body replacement device,Intervertebral fusion device with bone graft, cervical | 2 | ALEUTIAN® Interbody Systems |
| 21 | 10888857522107 | SP-4214-86 | SP-4214-86 | Trial Size 13x16x14 mm, 0° | MAX,MQP,ODP | Intervertebral fusion device with bone graft, lumbar,Spinal vertebral body repla Intervertebral fusion device with bone graft, lumbar,Spinal vertebral body replacement device,Intervertebral fusion device with bone graft, cervical | 2 | ALEUTIAN® Interbody Systems |
| 22 | 10888857522091 | SP-4214-85 | SP-4214-85 | Trial Size 13x16x13 mm, 0° | MQP,ODP,MAX | Spinal vertebral body replacement device,Intervertebral fusion device with bone Spinal vertebral body replacement device,Intervertebral fusion device with bone graft, cervical,Intervertebral fusion device with bone graft, lumbar | 2 | ALEUTIAN® Interbody Systems |
| 23 | 10888857522084 | SP-4214-84 | SP-4214-84 | Trial Size 13x16x12 mm, 0° | MAX,ODP,MQP | Intervertebral fusion device with bone graft, lumbar,Intervertebral fusion devic Intervertebral fusion device with bone graft, lumbar,Intervertebral fusion device with bone graft, cervical,Spinal vertebral body replacement device | 2 | ALEUTIAN® Interbody Systems |
| 24 | 10888857522077 | SP-4214-83 | SP-4214-83 | Trial Size 13x16x11 mm, 0° | MQP,ODP,MAX | Spinal vertebral body replacement device,Intervertebral fusion device with bone Spinal vertebral body replacement device,Intervertebral fusion device with bone graft, cervical,Intervertebral fusion device with bone graft, lumbar | 2 | ALEUTIAN® Interbody Systems |
| 25 | 10888857522060 | SP-4214-82 | SP-4214-82 | Trial Size 13x16x10 mm, 0° | MAX,ODP,MQP | Intervertebral fusion device with bone graft, lumbar,Intervertebral fusion devic Intervertebral fusion device with bone graft, lumbar,Intervertebral fusion device with bone graft, cervical,Spinal vertebral body replacement device | 2 | ALEUTIAN® Interbody Systems |
| 26 | 10888857522053 | SP-4214-81 | SP-4214-81 | Trial Size 13x16x9 mm, 0° | MAX,ODP,MQP | Intervertebral fusion device with bone graft, lumbar,Intervertebral fusion devic Intervertebral fusion device with bone graft, lumbar,Intervertebral fusion device with bone graft, cervical,Spinal vertebral body replacement device | 2 | ALEUTIAN® Interbody Systems |
| 27 | 10888857522046 | SP-4214-80 | SP-4214-80 | Trial Size 13x16x8 mm, 0° | MAX,MQP,ODP | Intervertebral fusion device with bone graft, lumbar,Spinal vertebral body repla Intervertebral fusion device with bone graft, lumbar,Spinal vertebral body replacement device,Intervertebral fusion device with bone graft, cervical | 2 | ALEUTIAN® Interbody Systems |
| 28 | 10888857522039 | SP-4214-79 | SP-4214-79 | Trial Size 13x16x7 mm, 0° | MQP,ODP,MAX | Spinal vertebral body replacement device,Intervertebral fusion device with bone Spinal vertebral body replacement device,Intervertebral fusion device with bone graft, cervical,Intervertebral fusion device with bone graft, lumbar | 2 | ALEUTIAN® Interbody Systems |
| 29 | 10888857559424 | PRO-1230-01 | PRO-1230-01 | Shaver | LXH | Orthopedic manual surgical instrument | 1 | ALEUTIAN Interbody Systems |
| 30 | 10888857522022 | SP-4214-78 | SP-4214-78 | Trial Size 13x16x6 mm, 0° | MAX,ODP,MQP | Intervertebral fusion device with bone graft, lumbar,Intervertebral fusion devic Intervertebral fusion device with bone graft, lumbar,Intervertebral fusion device with bone graft, cervical,Spinal vertebral body replacement device | 2 | ALEUTIAN® Interbody Systems |
| 31 | 10888857522015 | SP-4214-77 | SP-4214-77 | Trial Size 13x16x5 mm, 0° | ODP,MQP,MAX | Intervertebral fusion device with bone graft, cervical,Spinal vertebral body rep Intervertebral fusion device with bone graft, cervical,Spinal vertebral body replacement device,Intervertebral fusion device with bone graft, lumbar | 2 | ALEUTIAN® Interbody Systems |
| 32 | 10888857521766 | SP-4214-52 | SP-4214-52 | Trial Size 12x14x8 mm, 25° | ODP,MAX,MQP | Intervertebral fusion device with bone graft, cervical,Intervertebral fusion dev Intervertebral fusion device with bone graft, cervical,Intervertebral fusion device with bone graft, lumbar,Spinal vertebral body replacement device | 2 | ALEUTIAN® Interbody Systems |
| 33 | 10888857521261 | SP-4214-02 | SP-4214-02 | Trial Size 12x14x6 mm, 0° | ODP,MQP,MAX | Intervertebral fusion device with bone graft, cervical,Spinal vertebral body rep Intervertebral fusion device with bone graft, cervical,Spinal vertebral body replacement device,Intervertebral fusion device with bone graft, lumbar | 2 | ALEUTIAN® Interbody Systems |
| 34 | 10888857521254 | SP-4214-01 | SP-4214-01 | Trial Size 12x14x5 mm, 0° | MAX,ODP,MQP | Intervertebral fusion device with bone graft, lumbar,Intervertebral fusion devic Intervertebral fusion device with bone graft, lumbar,Intervertebral fusion device with bone graft, cervical,Spinal vertebral body replacement device | 2 | ALEUTIAN® Interbody Systems |
| 35 | 10888857515185 | SP-4031-03 | SP-4031-03 | Disc Scraper Size 8 mm | LXH | Orthopedic manual surgical instrument | 1 | ALEUTIAN Interbody Systems |
| 36 | 10888857515178 | SP-4031-02 | SP-4031-02 | Disc Scraper Size 7 mm | LXH | Orthopedic manual surgical instrument | 1 | ALEUTIAN Interbody Systems |
| 37 | 10888857515161 | SP-4031-01 | SP-4031-01 | Disc Scraper Size 6 mm | LXH | Orthopedic manual surgical instrument | 1 | ALEUTIAN Interbody Systems |
| 38 | 10888857494220 | SP-4232-02 | SP-4232-02 | Osteotome, Size 9 mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | ALEUTIAN® Interbody Systems |
| 39 | 10888857494213 | SP-4232-01 | SP-4232-01 | Osteotome, Size 8 mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | ALEUTIAN® Interbody Systems |
| 40 | 10888857469204 | SP-4013-09 | SP-4013-09 | Box Chisel, Size 15 mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | ALEUTIAN® Interbody Systems |
| 41 | 10888857469198 | SP-4013-08 | SP-4013-08 | Box Chisel, Size 14 mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | ALEUTIAN® Interbody Systems |
| 42 | 10888857469181 | SP-4013-07 | SP-4013-07 | Box Chisel, Size 13 mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | ALEUTIAN® Interbody Systems |
| 43 | 10888857469174 | SP-4013-06 | SP-4013-06 | Box Chisel, Size 12 mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | ALEUTIAN® Interbody Systems |
| 44 | 10888857469167 | SP-4013-05 | SP-4013-05 | Box Chisel, Size 11 mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | ALEUTIAN® Interbody Systems |
| 45 | 10888857469150 | SP-4013-04 | SP-4013-04 | Box Chisel, Size 10 mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | ALEUTIAN® Interbody Systems |
| 46 | 10888857469143 | SP-4013-03 | SP-4013-03 | Box Chisel, Size 9 mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | ALEUTIAN® Interbody Systems |
| 47 | 10888857469136 | SP-4013-02 | SP-4013-02 | Box Chisel, Size 8 mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | ALEUTIAN® Interbody Systems |
| 48 | 10888857469129 | SP-4013-01 | SP-4013-01 | Box Chisel, Size 7 mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | ALEUTIAN® Interbody Systems |
| 49 | 10888857559448 | PRO-1230-03 | PRO-1230-03 | Shaver | LXH | Orthopedic manual surgical instrument | 1 | ALEUTIAN Interbody Systems |
| 50 | 10888857559431 | PRO-1230-02 | PRO-1230-02 | Shaver | LXH | Orthopedic manual surgical instrument | 1 | ALEUTIAN Interbody Systems |
| No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
|---|---|---|---|---|---|---|
| 1 | 08806162199499 | 1108-0810 | 1108-0810 | "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 Cage | GS MEDICAL CO., LTD. |
| 2 | 08806162124255 | 1168-0816 | 1168-0816 | "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 Cage | GS MEDICAL CO., LTD. |
| 3 | 08806162124248 | 1168-0815 | 1168-0815 | "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 Cage | GS MEDICAL CO., LTD. |
| 4 | 08806162124231 | 1168-0814 | 1168-0814 | "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 Cage | GS MEDICAL CO., LTD. |
| 5 | 08806162124224 | 1168-0813 | 1168-0813 | "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 Cage | GS MEDICAL CO., LTD. |
| 6 | 08806162124217 | 1168-0812 | 1168-0812 | "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 Cage | GS MEDICAL CO., LTD. |
| 7 | 08806162124200 | 1168-0811 | 1168-0811 | "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 Cage | GS MEDICAL CO., LTD. |
| 8 | 08806162124194 | 1168-0810 | 1168-0810 | "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 Cage | GS MEDICAL CO., LTD. |
| 9 | 08806162124187 | 1148-0816 | 1148-0816 | "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 Cage | GS MEDICAL CO., LTD. |
| 10 | 08806162124170 | 1148-0815 | 1148-0815 | "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 Cage | GS MEDICAL CO., LTD. |
| 11 | 08806162124163 | 1148-0814 | 1148-0814 | "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 Cage | GS MEDICAL CO., LTD. |
| 12 | 08806162124156 | 1148-0813 | 1148-0813 | "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 Cage | GS MEDICAL CO., LTD. |
| 13 | 08806162124149 | 1148-0812 | 1148-0812 | "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 Cage | GS MEDICAL CO., LTD. |
| 14 | 08806162124132 | 1148-0811 | 1148-0811 | "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 Cage | GS MEDICAL CO., LTD. |
| 15 | 08806162124125 | 1148-0810 | 1148-0810 | "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 Cage | GS MEDICAL CO., LTD. |
| 16 | 08806162123951 | 1168-0416 | 1168-0416 | "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 Cage | GS MEDICAL CO., LTD. |
| 17 | 08806162123944 | 1168-0415 | 1168-0415 | "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 Cage | GS MEDICAL CO., LTD. |
| 18 | 08806162123937 | 1168-0414 | 1168-0414 | "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 Cage | GS MEDICAL CO., LTD. |
| 19 | 08806162123920 | 1168-0413 | 1168-0413 | "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 Cage | GS MEDICAL CO., LTD. |
| 20 | 08806162123913 | 1168-0412 | 1168-0412 | "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 Cage | GS MEDICAL CO., LTD. |
| 21 | 08806162123906 | 1168-0411 | 1168-0411 | "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 Cage | GS MEDICAL CO., LTD. |
| 22 | 08806162123890 | 1168-0410 | 1168-0410 | "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 Cage | GS MEDICAL CO., LTD. |
| 23 | 08806162123883 | 1168-0409 | 1168-0409 | "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 Cage | GS MEDICAL CO., LTD. |
| 24 | 08806162123869 | 1148-0416 | 1148-0416 | "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 Cage | GS MEDICAL CO., LTD. |
| 25 | 08806162123852 | 1148-0415 | 1148-0415 | "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 Cage | GS MEDICAL CO., LTD. |
| 26 | 08806162123845 | 1148-0414 | 1148-0414 | "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 Cage | GS MEDICAL CO., LTD. |
| 27 | 08806162123838 | 1148-0413 | 1148-0413 | "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 Cage | GS MEDICAL CO., LTD. |
| 28 | 08806162123821 | 1148-0412 | 1148-0412 | "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 Cage | GS MEDICAL CO., LTD. |
| 29 | 08806162123814 | 1148-0411 | 1148-0411 | "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 Cage | GS MEDICAL CO., LTD. |
| 30 | 08806162123807 | 1148-0410 | 1148-0410 | "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 Cage | GS MEDICAL CO., LTD. |
| 31 | 08806162123791 | 1148-0409 | 1148-0409 | "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 Cage | GS MEDICAL CO., LTD. |
| 32 | 08806162123784 | 1108-0416 | 1108-0416 | "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 Cage | GS MEDICAL CO., LTD. |
| 33 | 08806162123777 | 1108-0415 | 1108-0415 | "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 Cage | GS MEDICAL CO., LTD. |
| 34 | 08806162123760 | 1108-0414 | 1108-0414 | "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 Cage | GS MEDICAL CO., LTD. |
| 35 | 08806162123753 | 1108-0413 | 1108-0413 | "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 Cage | GS MEDICAL CO., LTD. |
| 36 | 08806162123746 | 1108-0412 | 1108-0412 | "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 Cage | GS MEDICAL CO., LTD. |
| 37 | 08806162123739 | 1108-0411 | 1108-0411 | "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 Cage | GS MEDICAL CO., LTD. |
| 38 | 08806162123722 | 1108-0410 | 1108-0410 | "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 Cage | GS MEDICAL CO., LTD. |
| 39 | 08806162123715 | 1108-0409 | 1108-0409 | "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 Cage | GS MEDICAL CO., LTD. |
| 40 | 08806162123500 | 1108-0015 | 1108-0015 | "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 Cage | GS MEDICAL CO., LTD. |
| 41 | 08806162121711 | 1109-1716 | 1109-1716 | "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 Cage | GS MEDICAL CO., LTD. |
| 42 | 08806162121704 | 1109-1715 | 1109-1715 | "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 Cage | GS MEDICAL CO., LTD. |
| 43 | 08806162121698 | 1109-1714 | 1109-1714 | "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 Cage | GS MEDICAL CO., LTD. |
| 44 | 08806162121681 | 1109-1713 | 1109-1713 | "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 Cage | GS MEDICAL CO., LTD. |
| 45 | 08806162121674 | 1109-1712 | 1109-1712 | "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 Cage | GS MEDICAL CO., LTD. |
| 46 | 08806162121667 | 1109-1711 | 1109-1711 | "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 Cage | GS MEDICAL CO., LTD. |
| 47 | 08806162121650 | 1109-1710 | 1109-1710 | "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 Cage | GS MEDICAL CO., LTD. |
| 48 | 08806162121643 | 1109-1709 | 1109-1709 | "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 Cage | GS MEDICAL CO., LTD. |
| 49 | 08806162121636 | 1109-1708 | 1109-1708 | "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 Cage | GS MEDICAL CO., LTD. |
| 50 | 08806162121629 | 1109-1707 | 1109-1707 | "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 Cage | GS MEDICAL CO., LTD. |