Other products from "HT MEDICAL, LLC"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00818345024748 23-LCN-3006 N/A Ti3D CAGE, 10W x 30L x 6H, 0 DEG, STRAIGHT MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 TIWAVE L
2 00818345024731 23-LCN-2806 N/A Ti3D CAGE, 10W x 28L x 6H, 0 DEG, STRAIGHT MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 TIWAVE L
3 00818345024724 23-LCN-2506 N/A Ti3D CAGE, 10W x 25L x 6H, 0 DEG, STRAIGHT MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 TIWAVE L
4 00818345024717 23-LCN-2206 N/A Ti3D CAGE, 10W x 22L x 6H, 0 DEG, STRAIGHT MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 TIWAVE L
5 00818345024700 23-LCN-2006 N/A Ti3D CAGE, 10W x 20L x 6H, 0 DEG, STRAIGHT MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 TIWAVE L
6 00818345027251 B04-02 Universal Handle, Cervical, Double Sided LXH Orthopedic Manual Surgical Instrument 1 Ti3D CERVICAL
7 00818345026773 C1412-04 Ti3D CAGE 14W x 12D x 4H, 6 DEG ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 NeoFuse Ti3D CERVICAL
8 00818345026261 20-RAT-9405 N/A CERVICAL RASP, 19 X 14 X 5MM, 7°, ANATOMIC LXH Orthopedic Manual Surgical Instrument 1 TIWAVE
9 00818345026254 20-RAT-7305 N/A CERVICAL RASP, 17 X 13 X 5MM, 7°, ANATOMIC LXH Orthopedic Manual Surgical Instrument 1 TIWAVE
10 00818345026247 20-RAT-5205 N/A CERVICAL RASP, 15 X 12 X 5MM, 7°, ANATOMIC LXH Orthopedic Manual Surgical Instrument 1 TIWAVE
11 00818345026230 20-RAT-3205 N/A CERVICAL RASP, 13 X 12 X 5MM, 7°, ANATOMIC LXH Orthopedic Manual Surgical Instrument 1 TIWAVE
12 00818345026223 20-RFT-9405 N/A CERVICAL RASP, 19 X 14 X 5MM, 7°, FLAT LXH Orthopedic Manual Surgical Instrument 1 TIWAVE
13 00818345026216 20-RFT-7305 N/A CERVICAL RASP, 17 X 13 X 5MM, 7°, FLAT LXH Orthopedic Manual Surgical Instrument 1 TIWAVE
14 00818345026209 20-RFT-5205 N/A CERVICAL RASP, 15 X 12 X 5MM, 7°, FLAT LXH Orthopedic Manual Surgical Instrument 1 TIWAVE
15 00818345026193 20-RFT-3205 N/A CERVICAL RASP, 13 X 12 X 5MM, 7°, FLAT LXH Orthopedic Manual Surgical Instrument 1 TIWAVE
16 00818345026186 20-CFT-9412 N/A TI3D CAGE, 19W X 12D X 12H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
17 00818345026179 20-CFT-9411 N/A TI3D CAGE, 19W X 12D X 11H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
18 00818345026162 20-CFT-9410 N/A TI3D CAGE, 19W X 12D X 10H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
19 00818345026155 20-CFT-9409 N/A TI3D CAGE, 19W X 12D X 9H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
20 00818345026148 20-CFT-9408 N/A TI3D CAGE, 19W X 12D X 8H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
21 00818345026131 20-CFT-9407 N/A TI3D CAGE, 19W X 12D X 7H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
22 00818345026124 20-CFT-9406 N/A TI3D CAGE, 19W X 12D X 6H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
23 00818345026117 20-CFT-9405 N/A TI3D CAGE, 19W X 12D X 5H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
24 00818345026032 C1211-04 Ti3D CAGE 12W x 11.5D x 4H, 6 DEG ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 NeoFuse Ti3D CERVICAL
25 00818345026025 20-CFX-5212 N/A Ti3D Cage, 15W x 12D x 12H, 14 Deg, Flat ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
26 00818345026018 20-CFX-5211 N/A Ti3D Cage, 15W x 12D x 11H, 14 Deg, Flat ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
27 00818345026001 20-CFX-5210 N/A Ti3D Cage, 15W x 12D x 10H, 14 Deg, Flat ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
28 00818345025998 20-CFX-5209 N/A Ti3D Cage, 15W x 12D x 9H, 14 Deg, Flat ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
29 00818345025981 20-CFX-5208 N/A Ti3D Cage, 15W x 12D x 8H, 14 Deg, Flat ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
30 00818345025974 20-CFX-5207 N/A Ti3D Cage, 15W x 12D x 7H, 14 Deg, Flat ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
31 00818345025967 20-CFX-5206 N/A Ti3D Cage, 15W x 12D x 6H, 14 Deg, Flat ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
32 00818345025950 20-CFX-5205 N/A Ti3D Cage, 15W x 12D x 5H, 14 Deg, Flat ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
33 00818345025943 20-CFT-7312 N/A TI3D CAGE, 17W X 12D X 12H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
34 00818345025936 20-CFT-7311 N/A TI3D CAGE, 17W X 12D X 11H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
35 00818345025929 20-CFT-7310 N/A TI3D CAGE, 17W X 12D X 10H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
36 00818345025912 20-CFT-7309 N/A TI3D CAGE, 17W X 12D X 9H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
37 00818345025905 20-CFT-7308 N/A TI3D CAGE, 17W X 12D X 8H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
38 00818345025899 20-CFT-7307 N/A TI3D CAGE, 17W X 12D X 7H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
39 00818345025882 20-CFT-7306 N/A TI3D CAGE, 17W X 12D X 6H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
40 00818345025875 20-CFT-7305 N/A TI3D CAGE, 17W X 12D X 5H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
41 00818345025868 20-CFT-5212 N/A TI3D CAGE, 15W X 12D X 12H, 7DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
42 00818345025851 20-CFT-5211 N/A TI3D CAGE, 15W X 12D X 11H, 7DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
43 00818345025844 20-CFT-5210 N/A TI3D CAGE, 15W X 12D X 10H, 7DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
44 00818345025837 20-CFT-5209 N/A TI3D CAGE, 15W X 12D X 9H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
45 00818345025820 20-CFT-5208 N/A TI3D CAGE, 15W X 12D X 8H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
46 00818345025813 20-CFT-5207 N/A TI3D CAGE, 15W X 12D X 7H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
47 00818345025806 20-CFT-5206 N/A TI3D CAGE, 15W X 12D X 6H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
48 00818345025790 20-CFT-5205 N/A TI3D CAGE, 15W X 12D X 5H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
49 00818345025783 20-CFT-3212 N/A TI3D CAGE, 13W X 12D X 12H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
50 00818345025776 20-CFT-3211 N/A TI3D CAGE, 13W X 12D X 11H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
Other products with the same Product Code "MAX"
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