Other products from "INNOVASIS, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 M711CRT006ST0 CRT006ST CP Ti GWO Plate, Cranioplasty, Preformed, Alterable 2 Neuro & Craniofacial Fixation System
2 M711E20024 E2002 E2002 KWQ,KWP,MNH,MNI,NKB Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Inte Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease Excella II®
3 M711BTA1190 BTA-119 Al, SST, Nylon, Silicone LXH Orthopedic Manual Surgical Instrument 1 PSO
4 M711X212163200 X21216320 X21216320 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
5 M711X212163000 X21216300 X21216300 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
6 M711X212162800 X21216280 X21216280 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
7 M711X212153200 X21215320 X21215320 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
8 M711X212153000 X21215300 X21215300 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
9 M711X212152800 X21215280 X21215280 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
10 M711X212143200 X21214320 X21214320 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
11 M711X212143000 X21214300 X21214300 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
12 M711X212142800 X21214280 X21214280 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
13 M711X212133200 X21213320 X21213320 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
14 M711X212133000 X21213300 X21213300 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
15 M711X212132800 X21213280 X21213280 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
16 M711X212123200 X21212320 X21212320 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
17 M711X212123000 X21212300 X21212300 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
18 M711X212122800 X21212280 X21212280 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
19 M711X212113200 X21211320 X21211320 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
20 M711X212113000 X21211300 X21211300 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
21 M711X212112800 X21211280 X21211280 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
22 M711X212103200 X21210320 X21210320 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
23 M711X212103000 X21210300 X21210300 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
24 M711X212102800 X21210280 X21210280 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
25 M711X212093200 X21209320 X21209320 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
26 M711X212093000 X21209300 X21209300 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
27 M711X212092800 X21209280 X21209280 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
28 M711X212082800 X21208280 X21208280 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
29 M711X210162550 X21016255 X21016255 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
30 M711X210162500 X21016250 X21016250 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
31 M711X210162250 X21016225 X21016225 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
32 M711X210162200 X21016220 X21016220 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
33 M711X210153200 X21015320 X21015320 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
34 M711X210152800 X21015280 X21015280 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
35 M711X210152550 X21015255 X21015255 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
36 M711X210152500 X21015250 X21015250 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
37 M711X210152250 X21015225 X21015225 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
38 M711X210152200 X21015220 X21015220 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
39 M711X210143200 X21014320 X21014320 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
40 M711X210142800 X21014280 X21014280 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
41 M711X210142550 X21014255 X21014255 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
42 M711X210142500 X21014250 X21014250 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
43 M711X210142250 X21014225 X21014225 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
44 M711X210142200 X21014220 X21014220 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
45 M711X210133200 X21013320 X21013320 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
46 M711X210132800 X21013280 X21013280 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
47 M711X210132550 X21013255 X21013255 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
48 M711X210132500 X21013250 X21013250 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
49 M711X210132250 X21013225 X21013225 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
50 M711X210132200 X21013220 X21013220 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
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