No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 07640305160226 | MPF-IN 04 00-N | MPF-IN 04 00-N | TROCAR AWL | KWP,NKB | Appliance, Fixation, Spinal Interlaminal,Thoracolumbosacral Pedicle Screw System | 2 | PERLA ® TL MIS |
2 | 07640151087623 | PAD-IM TI 16-S | Posterior Axial Device - Titanium | PEK | Spinous Process Plate | 2 | ROMEO 2 PAD POSTERIOR AXIAL DEVICE | |
3 | 07640151087609 | PAD-IM TI 12-S | Posterior Axial Device - Titanium | PEK | Spinous Process Plate | 2 | ROMEO 2 PAD POSTERIOR AXIAL DEVICE | |
4 | 07640151084073 | ELL-CC MU 43-S | Cross Connector / Multiaxial | MNH,MNI,KWP | Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Ap Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | ROMEO Posterior Osteosynthesis system | |
5 | 07640178975262 | CPF-IN 22 02-N | CPF-IN 22 02-N | Screwdriver Tube | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PERLA ® |
6 | 07640151082970 | ELL-DS 07 35-S | 25D Screw | MNH,MNI,KWP | Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Ap Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | ROMEO Posterior Osteosynthesis system | |
7 | 07640151082949 | ELL-DS 06 80-S | 25D Screw | MNH,MNI,KWP | Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Ap Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | ROMEO Posterior Osteosynthesis system | |
8 | 07640151082925 | ELL-DS 06 60-S | 25D Screw | MNH,MNI,KWP | Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Ap Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | ROMEO Posterior Osteosynthesis system | |
9 | 07640450863447 | TRY-IN 51 01-N | TRY-IN 51 01-N | 3D PRINTED HAN | ODP | Intervertebral Fusion Device With Bone Graft, Cervical | 2 | TRYPTIK ® TI |
10 | 07640151082833 | ELL-DS 55 45-S | 25D Screw | MNH,MNI,KWP | Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Ap Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | ROMEO Posterior Osteosynthesis system | |
11 | 07640450860989 | TLF-SC 00 00-N | TLF-SC 00 00-N | SETSCREW | KWP,NKB | Appliance, Fixation, Spinal Interlaminal,Thoracolumbosacral Pedicle Screw System | 2 | PERLA ® TL |
12 | 07640151082819 | ELL-DS 55 35-S | 25D Screw | MNH,MNI,KWP | Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Ap Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | ROMEO Posterior Osteosynthesis system | |
13 | 07640151082772 | ELL-DS 05 40-S | 25D Screw | MNH,MNI,KWP | Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Ap Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | ROMEO Posterior Osteosynthesis system | |
14 | 07640151082703 | ELL-DS 45 25-S | 25D Screw | MNH,MNI,KWP | Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Ap Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | ROMEO Posterior Osteosynthesis system | |
15 | 07640151082680 | ELL-DS 04 40-S | 25D Screw | MNH,MNI,KWP | Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Ap Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | ROMEO Posterior Osteosynthesis system | |
16 | 07640151082659 | ELL-DS 04 25-S | 25D Screw | MNH,MNI,KWP | Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Ap Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | ROMEO Posterior Osteosynthesis system | |
17 | 07640151081928 | ELL-RD 13 50-S | Rod Cobalt Chromium / Straight | KWP,MNH,MNI | Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixa Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | ROMEO Posterior Osteosynthesis system | |
18 | 07640305160899 | MPF-PX 65 30-S | MPF-PX 65 30-S | XTAB CANNULATED POLYAXIAL SCREW | KWP,NKB | Appliance, Fixation, Spinal Interlaminal,Thoracolumbosacral Pedicle Screw System | 2 | PERLA ® TL MIS |
19 | 07640178975200 | CPF-IN 17 00-N | CPF-IN 17 00-N | Pusher | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PERLA ® |
20 | 07640185341722 | SPE-US 00 40-N | SPE-US 00 40-N | ANGLED TAP | HWX | Tap, Bone | 1 | SCARLET AC-T |
21 | 07640178984981 | MIS-IN 52 10-N | Trocar Handle | HWJ | Awl | 1 | ROMEO 2 MIS | |
22 | 07640178985704 | SPE-US 00 28-N | SPE-US 00 28-N | ROD HOLDER | NKG,KWP | Orthosis, Cervical Pedicle Screw Spinal Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | PERLA ® |
23 | 07640178981584 | JUT-IN 03 12-N | JUT-IN 03 12-N | TRIAL IMPLANT Ti TL | HWT | Template | 1 | JULIET ® INSTRUMENTATION |
24 | 07640178980662 | JUL-LT 6S 8C-S | JUL-LT 6S 8C-S | JUL-LT 6S 8C-S | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | JULIET ® LL |
25 | 07640178975934 | CPF-SS 04 22-S | CPF-SS 04 22-S | NKG,KWP | Orthosis, Cervical Pedicle Screw Spinal Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | PERLA ® | |
26 | 07640151081225 | TRY-AC 12 09-S | Cervical Cage / Convex | ODP | Intervertebral Fusion Device With Bone Graft, Cervical | 2 | TRYPTIK Anterior Intersomatic Cervical cage | |
27 | 07640151081010 | TRY-CL 14 12-S | Cervical Cage / Lordotic | ODP | Intervertebral Fusion Device With Bone Graft, Cervical | 2 | TRYPTIK Anterior Intersomatic Cervical cage | |
28 | 07640178971301 | ELL-R6 15 50-S | Rod Cobalt Chromium / Prebent | MNI,MNH | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation | 2 | ROMEO Posterior Osteosynthesis system | |
29 | 07640151080969 | TRY-CL 14 07-S | Cervical Cage / Lordotic | ODP | Intervertebral Fusion Device With Bone Graft, Cervical | 2 | TRYPTIK Anterior Intersomatic Cervical cage | |
30 | 07640151080952 | TRY-CL 14 06-S | Cervical Cage / Lordotic | ODP | Intervertebral Fusion Device With Bone Graft, Cervical | 2 | TRYPTIK Anterior Intersomatic Cervical cage | |
31 | 07640151080945 | TRY-CL 14 05-S | Cervical Cage / Lordotic | ODP | Intervertebral Fusion Device With Bone Graft, Cervical | 2 | TRYPTIK Anterior Intersomatic Cervical cage | |
32 | 07640151112578 | JLL-IN 06 08-N | JLL-IN 06 08-N | PADDLE SHAVER 8 | LWK | Razor, Surgical | 1 | JULIET ® INSTRUMENTATION |
33 | 07640151096304 | CPF-CS 04 52-S | CC PREFERRED ANGLE SCREW | NKG,KWP | Orthosis, Cervical Pedicle Screw Spinal Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | PERLA ® | |
34 | 07640151095239 | CPF-IN 20 00-N | CPF-IN 20 00-N | Rocker | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PERLA ® |
35 | 07640151092597 | JUL-IN 19 10-N | JUL-IN 19 10-N | Paddle Shaver H10 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | JULIET INSTRUMENTATION |
36 | 07640139346179 | ELL-RD 10 30-S | KWP,MNH,MNI | Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixa Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | ROMEO Posterior Osteosynthesis System | ||
37 | 07640139345455 | ELL-PS 45 45-S | Polyaxial Screw | KWP,MNH,MNI | Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixa Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | ROMEO Posterior Osteosynthesis System | |
38 | 07640139345448 | ELL-PS 45 40-S | Polyaxial Screw | KWP,MNH,MNI | Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixa Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | ROMEO Posterior Osteosynthesis System | |
39 | 07640151089474 | OTO-BC 09 02-N | OTO-BC 09 02-N | RETRACTOR BLADE | GAD | Retractor | 1 | OTELO INSTRUMENTATION |
40 | 07640151087579 | ELL-IN 05 06-N | ELL-IN 05 06-N | K-WIRE BLUNT - NITINOLFINAL TIGHTENER | KWP,MNH,MNI | Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixa Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | ROMEO 2 INSTRUMENTATION |
41 | 07640139345424 | ELL-PS 45 30-S | Polyaxial Screw | KWP,MNH,MNI | Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixa Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | ROMEO Posterior Osteosynthesis System | |
42 | 07640151083021 | ELL-DS 07 55-S | 25D Screw | MNH,MNI,KWP | Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Ap Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | ROMEO Posterior Osteosynthesis system | |
43 | 07640151080846 | ELL-IN 01 34-N | ELL-IN 01 34-N | REDUCER T-HANDLE | HWN,MNI,MNH | Instrument, Compression,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolist Instrument, Compression,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation | 1 | ROMEO 2 INSTRUMENTATION |
44 | 07640139347329 | ELL-RD 30 30-S | Rod Straight | KWP,MNH,MNI | Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixa Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | ROMEO Posterior Osteosynthesis System | |
45 | 07640139346193 | ELL-RD 10 50-S | Rod Cobalt Chromium / Prebent | KWP,MNH,MNI | Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixa Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | ROMEO Posterior Osteosynthesis System | |
46 | 07640139347404 | ELL-RD 30 90-S | Rod Straight | KWP,MNH,MNI | Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixa Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | ROMEO Posterior Osteosynthesis System | |
47 | 07640139347213 | ELL-PS 06 90-S | Polyaxial Screw | KWP,MNH,MNI | Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixa Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | ROMEO Posterior Osteosynthesis System | |
48 | 07640139345769 | ELL-PS 07 80-S | Polyaxial Screw | KWP,MNH,MNI | Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixa Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | ROMEO Posterior Osteosynthesis System | |
49 | 07640139343970 | ELL-MS 45 25-S | Monoaxial Screw | KWP,MNH,MNI | Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixa Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | ROMEO Posterior Osteosynthesis system | |
50 | 07640139340061 | MOS-CA 14 07-S | Cervical Cage | ODP | Intervertebral Fusion Device With Bone Graft, Cervical | 2 | TRYPTIK CA ANTERIOR INTERSOMATIC CERVICAL CAGE |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 08806395422111 | 1189-1665 | 1189-1665 | "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 | 08806395422104 | 1189-1265 | 1189-1265 | "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 | 08806395422098 | 1189-1265 | 1189-1265 | "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 | 08806395422081 | 1189-1065 | 1189-1065 | "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 | 08806395422074 | 1189-0865 | 1189-0865 | "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 | 08806395422067 | 1189-1660 | 1189-1660 | "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 | 08806395422050 | 1189-1460 | 1189-1460 | "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 | 08806395422043 | 1189-1260 | 1189-1260 | "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 | 08806395422036 | 1189-1060 | 1189-1060 | "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 | 08806395422029 | 1189-0860 | 1189-0860 | "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 | 08806395422012 | 1189-1655 | 1189-1655 | "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. |
12 | 08806395422005 | 1189-1455 | 1189-1455 | "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. |
13 | 08806395421992 | 1189-1255 | 1189-1255 | "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. |
14 | 08806395421985 | 1189-1055 | 1189-1055 | "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. |
15 | 08806395421978 | 1189-0855 | 1189-0855 | "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. |
16 | 08806395421961 | 1189-1650 | 1189-1650 | "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. |
17 | 08806395421954 | 1189-1450 | 1189-1450 | "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. |
18 | 08806395421947 | 1189-1250 | 1189-1250 | "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. |
19 | 08806395421930 | 1189-1050 | 1189-1050 | "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. |
20 | 08806395421923 | 1189-0850 | 1189-0850 | "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. |
21 | 08806395421916 | 1189-1645 | 1189-1645 | "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. |
22 | 08806395421909 | 1189-1445 | 1189-1445 | "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. |
23 | 08806395421893 | 1189-1245 | 1189-1245 | "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. |
24 | 08806395421886 | 1189-1045 | 1189-1045 | "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. |
25 | 08806395421879 | 1189-0845 | 1189-0845 | "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. |
26 | 08806395421862 | 1189-1640 | 1189-1640 | "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. |
27 | 08806395421855 | 1189-1440 | 1189-1440 | "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. |
28 | 08806395421848 | 1189-1240 | 1189-1240 | "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. |
29 | 08806395421831 | 1189-1040 | 1189-1040 | "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. |
30 | 08806395421824 | 1189-0840 | 1189-0840 | "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. |
31 | 08806395421817 | 1282-1665 | 1282-1665 | "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 | 08806395421800 | 1282-1465 | 1282-1465 | "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 | 08806395421794 | 1282-1265 | 1282-1265 | "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 | 08806395421787 | 1282-1065 | 1282-1065 | "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 | 08806395421770 | 1282-0865 | 1282-0865 | "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 | 08806395421763 | 1282-1660 | 1282-1660 | "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 | 08806395421756 | 1282-1460 | 1282-1460 | "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 | 08806395421749 | 1282-1260 | 1282-1260 | "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 | 08806395421732 | 1282-1060 | 1282-1060 | "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 | 08806395421725 | 1282-0860 | 1282-0860 | "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 | 08806395421718 | 1282-1655 | 1282-1655 | "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. |
42 | 08806395421701 | 1282-1455 | 1282-1455 | "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. |
43 | 08806395421695 | 1282-1255 | 1282-1255 | "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. |
44 | 08806395421688 | 1282-1055 | 1282-1055 | "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. |
45 | 08806395421671 | 1282-0855 | 1282-0855 | "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. |
46 | 08806395421664 | 1282-1650 | 1282-1650 | "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. |
47 | 08806395421657 | 1282-1450 | 1282-1450 | "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. |
48 | 08806395421640 | 1282-1250 | 1282-1250 | "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. |
49 | 08806395421633 | 1282-1050 | 1282-1050 | "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. |
50 | 08806395421626 | 1282-0850 | 1282-0850 | "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. |