No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 00853896008328 | ZF-300-3011 | ZF-300-3011 | TLIF Spacer 30mm Long x 11mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
2 | 00853896008410 | ZF-300-3008 | ZF-300-3008 | TLIF Spacer 30mm Long x 8mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
3 | 00853896008403 | ZF-300-2711 | ZF-300-2711 | TLIF Spacer 27mm Long x 11mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
4 | 00853896008397 | ZF-300-2714 | ZF-300-2714 | TLIF Spacer 27mm Long x 14mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
5 | 00853896008380 | ZF-300-2713 | ZF-300-2713 | TLIF Spacer 27mm Long x 13mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
6 | 00853896008373 | ZF-300-2712 | ZF-300-2712 | TLIF Spacer 27mm Long x 12mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
7 | 00853896008366 | ZF-300-2710 | ZF-300-2710 | TLIF Spacer 27mm Long x 10mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
8 | 00853896008359 | ZF-300-3014 | ZF-300-3014 | TLIF Spacer 30mm Long x 14mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
9 | 00853896008335 | ZF-300-3012 | ZF-300-3012 | TLIF Spacer 30mm Long x 12mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
10 | 00853896008311 | ZF-300-3010 | ZF-300-3010 | TLIF Spacer 30mm Long x 10mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
11 | 00853896008304 | ZF-300-3009 | ZF-300-3009 | TLIF Spacer 30mm Long x 9mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
12 | 00853896008298 | ZF-300-2709 | ZF-300-2709 | TLIF Spacer 27mm Long x 9mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
13 | 00853896008281 | ZF-300-2708 | ZF-300-2708 | TLIF Spacer 27mm Long x 8mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
14 | 00853896008274 | ZF-300-2414 | ZF-300-2414 | TLIF Spacer 24mm Long x 14mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
15 | 00853896008267 | ZF-300-2413 | ZF-300-2413 | TLIF Spacer 24mm Long x 13mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
16 | 00853896008250 | ZF-300-2412 | ZF-300-2412 | TLIF Spacer 24mm Long x 12mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
17 | 00853896008243 | ZF-300-2411 | ZF-300-2411 | TLIF Spacer 24mm Long x 11mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
18 | 00853896008236 | ZF-300-2410 | ZF-300-2410 | TLIF Spacer 24mm Long x 10mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
19 | 00853896008229 | ZF-300-2409 | ZF-300-2409 | TLIF Spacer 24mm Long x 9mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
20 | 00853896008212 | ZF-300-2408 | ZF-300-2408 | TLIF Spacer 24mm Long x 8mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
21 | 00853896008205 | ZF-100-2914 | ZF-100-2914 | PLIF Spacer 29mm Long x 14mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
22 | 00853896008199 | ZF-100-2913 | ZF-100-2913 | PLIF Spacer 29mm Long x 13mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
23 | 00853896008182 | ZF-100-2912 | ZF-100-2912 | PLIF Spacer 29mm Long x 12mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
24 | 00853896008175 | ZF-100-2911 | ZF-100-2911 | PLIF Spacer 29mm Long x 11mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
25 | 00853896008168 | ZF-100-2910 | ZF-100-2910 | PLIF Spacer 29mm Long x 10mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
26 | 00853896008151 | ZF-100-2909 | ZF-100-2909 | PLIF Spacer 29mm Long x 9mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
27 | 00853896008144 | ZF-100-2908 | ZF-100-2908 | PLIF Spacer 29mm Long x 8mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
28 | 00853896008137 | ZF-100-2614 | ZF-100-2614 | PLIF Spacer 26mm Long x 14mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
29 | 00853896008120 | ZF-100-2613 | ZF-100-2613 | PLIF Spacer 26mm Long x 13mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
30 | 00853896008113 | ZF-100-2612 | ZF-100-2612 | PLIF Spacer 26mm Long x 12mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
31 | 00853896008106 | ZF-100-2611 | ZF-100-2611 | PLIF Spacer 26mm Long x 11mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
32 | 00853896008090 | ZF-100-2610 | ZF-100-2610 | PLIF Spacer 26mm Long x 10mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
33 | 00853896008083 | ZF-100-2609 | ZF-100-2609 | PLIF Spacer 26mm Long x 9mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
34 | 00853896008076 | ZF-100-2608 | ZF-100-2608 | PLIF Spacer 26mm Long x 8mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
35 | 00853896008069 | ZF-100-2214 | ZF-100-2214 | PLIF Spacer 22mm Long x 14mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
36 | 00853896008052 | ZF-100-2213 | ZF-100-2213 | PLIF Spacer 22mm Long x 13mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
37 | 00853896008045 | ZF-100-2212 | ZF-100-2212 | PLIF Spacer 22mm Long x 12mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
38 | 00853896008038 | ZF-100-2210 | ZF-100-2210 | PLIF Spacer 22mm Long x 10mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
39 | 00853896008021 | ZF-100-2209 | ZF-100-2209 | PLIF Spacer 22mm Long x 9mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
40 | 00853896008014 | ZF-100-2208 | ZF-100-2208 | PLIF Spacer 22mm Long x 8mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
41 | 00853896008007 | ZF-100-2211 | ZF-100-2211 | PLIF Spacer 22mm Long x 11mm Height | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | XIPHOS ZFUZE |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 08806378300900 | 1101-1012 | 1101-1012 | "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 | 08806378300894 | 1101-1011 | 1101-1011 | "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 | 08806378300887 | 1101-1010 | 1101-1010 | "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 | 08806378300870 | 1101-1009 | 1101-1009 | "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 | 08806378300863 | 1101-1008 | 1101-1008 | "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 | 08806373874192 | SI.C10.0010 | ACIF HOLDER STOPPER TYPE | LOSPA IS Spinal System | CORENTEC CO., LTD | |
7 | 08806373871825 | SI.C50.6816 | T-PLIF TRIAL 8° 34 X 10 X 16 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
8 | 08806373871818 | SI.C50.6815 | T-PLIF TRIAL 8° 34 X 10 X 15 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
9 | 08806373871801 | SI.C50.6814 | T-PLIF TRIAL 8° 34 X 10 X 14 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
10 | 08806373871795 | SI.C50.6813 | T-PLIF TRIAL 8° 34 X 10 X 13 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
11 | 08806373871788 | SI.C50.6812 | T-PLIF TRIAL 8° 34 X 10 X 12 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
12 | 08806373871771 | SI.C50.6416 | T-PLIF TRIAL 4° 34 X 10 X 16 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
13 | 08806373871764 | SI.C50.6415 | T-PLIF TRIAL 4° 34 X 10 X 15 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
14 | 08806373871757 | SI.C50.6414 | T-PLIF TRIAL 4° 34 X 10 X 14 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
15 | 08806373871740 | SI.C50.6413 | T-PLIF TRIAL 4° 34 X 10 X 13 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
16 | 08806373871733 | SI.C50.6412 | T-PLIF TRIAL 4° 34 X 10 X 12 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
17 | 08806373871726 | SI.C50.6411 | T-PLIF TRIAL 4° 34 X 10 X 11 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
18 | 08806373871719 | SI.C50.6410 | T-PLIF TRIAL 4° 34 X 10 X 10 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
19 | 08806373871702 | SI.C50.6409 | T-PLIF TRIAL 4° 34 X 10 X 09 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
20 | 08806373871696 | SI.C50.6016 | T-PLIF TRIAL 0° 34 X 10 X 16 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
21 | 08806373871689 | SI.C50.6015 | T-PLIF TRIAL 0° 34 X 10 X 15 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
22 | 08806373871672 | SI.C50.6014 | T-PLIF TRIAL 0° 34 X 10 X 14 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
23 | 08806373871665 | SI.C50.6013 | T-PLIF TRIAL 0° 34 X 10 X 13 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
24 | 08806373871658 | SI.C50.6012 | T-PLIF TRIAL 0° 34 X 10 X 12 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
25 | 08806373871641 | SI.C50.6011 | T-PLIF TRIAL 0° 34 X 10 X 11 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
26 | 08806373871634 | SI.C50.6010 | T-PLIF TRIAL 0° 34 X 10 X 10 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
27 | 08806373871627 | SI.C50.6009 | T-PLIF TRIAL 0° 34 X 10 X 09 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
28 | 08806373871610 | SI.C50.6008 | T-PLIF TRIAL 0° 34 X 10 X 08 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
29 | 08806373871603 | SI.C50.5816 | T-PLIF TRIAL 8° 31 X 10 X 16 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
30 | 08806373871597 | SI.C50.5815 | T-PLIF TRIAL 8° 31 X 10 X 15 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
31 | 08806373871580 | SI.C50.5814 | T-PLIF TRIAL 8° 31 X 10 X 14 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
32 | 08806373871573 | SI.C50.5813 | T-PLIF TRIAL 8° 31 X 10 X 13 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
33 | 08806373871566 | SI.C50.5812 | T-PLIF TRIAL 8° 31 X 10 X 12 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
34 | 08806373871559 | SI.C50.5811 | T-PLIF TRIAL 8° 31 X 10 X 11 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
35 | 08806373871542 | SI.C50.5810 | T-PLIF TRIAL 8° 31 X 10 X 10 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
36 | 08806373871535 | SI.C50.5416 | T-PLIF TRIAL 4° 31 X 10 X 16 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
37 | 08806373871528 | SI.C50.5415 | T-PLIF TRIAL 4° 31 X 10 X 15 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
38 | 08806373871511 | SI.C50.5414 | T-PLIF TRIAL 4° 31 X 10 X 14 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
39 | 08806373871504 | SI.C50.5413 | T-PLIF TRIAL 4° 31 X 10 X 13 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
40 | 08806373871498 | SI.C50.5412 | T-PLIF TRIAL 4° 31 X 10 X 12 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
41 | 08806373871481 | SI.C50.5411 | T-PLIF TRIAL 4° 31 X 10 X 11 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
42 | 08806373871474 | SI.C50.5410 | T-PLIF TRIAL 4° 31 X 10 X 10 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
43 | 08806373871467 | SI.C50.5409 | T-PLIF TRIAL 4° 31 X 10 X 09 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
44 | 08806373871450 | SI.C50.5016 | T-PLIF TRIAL 0° 31 X 10 X 16 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
45 | 08806373871443 | SI.C50.5015 | T-PLIF TRIAL 0° 31 X 10 X 15 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
46 | 08806373871436 | SI.C50.5014 | T-PLIF TRIAL 0° 31 X 10 X 14 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
47 | 08806373871429 | SI.C50.5013 | T-PLIF TRIAL 0° 31 X 10 X 13 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
48 | 08806373871412 | SI.C50.5012 | T-PLIF TRIAL 0° 31 X 10 X 12 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
49 | 08806373871405 | SI.C50.5011 | T-PLIF TRIAL 0° 31 X 10 X 11 | LOSPA IS Spinal System | CORENTEC CO., LTD | |
50 | 08806373871399 | SI.C50.5010 | T-PLIF TRIAL 0° 31 X 10 X 10 | LOSPA IS Spinal System | CORENTEC CO., LTD |