Other products from "PIONEER SURGICAL TECHNOLOGY, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00846468099992 02-95SCREW-CDY 02-95SCREW-CDY SCREW CADDY FSM TRAY, SURGICAL, INSTRUMENT 1 Streamline TL Spinal Fixation System
2 00846468099985 02-CASE-DEF-EMPTY1 02-CASE-DEF-EMPTY1 Instrument Case 1 FSM TRAY, SURGICAL, INSTRUMENT 1 Streamline TL Spinal Fixation System
3 00846468099978 02-CASE-DEF-EMPTY2 02-CASE-DEF-EMPTY2 Instrument Case 2 FSM TRAY, SURGICAL, INSTRUMENT 1 Streamline TL Spinal Fixation System
4 00846468099961 02-FX-AUXCDY-E 02-FX-AUXCDY-E Auxiliary Screw Caddy, Fixed, Empty FSM TRAY, SURGICAL, INSTRUMENT 1 Streamline TL Spinal Fixation System
5 00846468099954 02-LID-RC-LNG 02-LID-RC-LNG Replacement Lid, Long Rod Caddy FSM TRAY, SURGICAL, INSTRUMENT 1 Streamline TL Spinal Fixation System
6 00846468099947 65-C-TRL-M-9-6L 65-C-TRL-M-9-6L Trial Spacer HWT TEMPLATE 1 Fortilink-C IBF System
7 00846468099930 725-133 725-133 FORTILINK-TS, PISTOL GRIP INSERTER LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 Fortilink-TS IBFSystem
8 00846468099848 65-C-TRL-L-11-10L 65-C-TRL-L-11-10L TRIAL SPACER HWT TEMPLATE 1 Fortilink-C IBF System
9 00846468099831 65-C-TRL-L-10-10L 65-C-TRL-L-10-10L TRIAL SPACER HWT TEMPLATE 1 Fortilink-C IBF System
10 00846468099824 65-C-TRL-L-9-10L 65-C-TRL-L-9-10L TRIAL SPACER HWT TEMPLATE 1 Fortilink-C IBF System
11 00846468099817 65-C-TRL-L-8-10L 65-C-TRL-L-8-10L TRIAL SPACER HWT TEMPLATE 1 Fortilink-C IBF System
12 00846468099800 65-C-TRL-L-7-10L 65-C-TRL-L-7-10L TRIAL SPACER HWT TEMPLATE 1 Fortilink-C IBF System
13 00846468099794 65-C-TRL-L-6-10L 65-C-TRL-L-6-10L TRIAL SPACER HWT TEMPLATE 1 Fortilink-C IBF System
14 00846468099787 65-C-TRL-M-11-10L 65-C-TRL-M-11-10L TRIAL SPACER HWT TEMPLATE 1 Fortilink-C IBF System
15 00846468099770 65-C-TRL-M-10-10L 65-C-TRL-M-10-10L TRIAL SPACER HWT TEMPLATE 1 Fortilink-C IBF System
16 00846468099763 65-C-TRL-M-9-10L 65-C-TRL-M-9-10L TRIAL SPACER HWT TEMPLATE 1 Fortilink-C IBF System
17 00846468099756 65-C-TRL-M-8-10L 65-C-TRL-M-8-10L TRIAL SPACER HWT TEMPLATE 1 Fortilink-C IBF System
18 00846468099749 65-C-TRL-M-7-10L 65-C-TRL-M-7-10L TRIAL SPACER HWT TEMPLATE 1 Fortilink-C IBF System
19 00846468099732 65-C-TRL-M-6-10L 65-C-TRL-M-6-10L TRIAL SPACER HWT TEMPLATE 1 Fortilink-C IBF System
20 00846468099725 65-C-TRL-S-11-10L 65-C-TRL-S-11-10L TRIAL SPACER HWT TEMPLATE 1 Fortilink-C IBF System
21 00846468099718 65-C-TRL-S-10-10L 65-C-TRL-S-10-10L TRIAL SPACER HWT TEMPLATE 1 Fortilink-C IBF System
22 00846468099701 65-C-TRL-S-9-10L 65-C-TRL-S-9-10L TRIAL SPACER HWT TEMPLATE 1 Fortilink-C IBF System
23 00846468099695 65-C-TRL-S-8-10L 65-C-TRL-S-8-10L TRIAL SPACER HWT TEMPLATE 1 Fortilink-C IBF System
24 00846468099688 65-C-TRL-S-7-10L 65-C-TRL-S-7-10L TRIAL SPACER HWT TEMPLATE 1 Fortilink-C IBF System
25 00846468099671 65-C-TRL-S-6-10L 65-C-TRL-S-6-10L TRIAL SPACER HWT TEMPLATE 1 Fortilink-C IBF System
26 00846468099602 65-C-TRL-L-11-6L 65-C-TRL-L-11-6L Trial Spacer HWT TEMPLATE 1 Fortilink-C IBF System
27 00846468099596 65-C-TRL-L-10-6L 65-C-TRL-L-10-6L Trial Spacer HWT TEMPLATE 1 Fortilink-C IBF System
28 00846468099589 65-C-TRL-L-9-6L 65-C-TRL-L-9-6L Trial Spacer HWT TEMPLATE 1 Fortilink-C IBF System
29 00846468099572 65-C-TRL-L-8-6L 65-C-TRL-L-8-6L Trial Spacer HWT TEMPLATE 1 Fortilink-C IBF System
30 00846468099565 65-C-TRL-L-7-6L 65-C-TRL-L-7-6L Trial Spacer HWT TEMPLATE 1 Fortilink-C IBF System
31 00846468099558 65-C-TRL-L-6-6L 65-C-TRL-L-6-6L Trial Spacer HWT TEMPLATE 1 Fortilink-C IBF System
32 00846468099541 65-C-TRL-L-5-6L 65-C-TRL-L-5-6L Trial Spacer HWT TEMPLATE 1 Fortilink-C IBF System
33 00846468099534 65-C-TRL-M-11-6L 65-C-TRL-M-11-6L Trial Spacer HWT TEMPLATE 1 Fortilink-C IBF System
34 00846468099527 65-C-TRL-M-10-6L 65-C-TRL-M-10-6L Trial Spacer HWT TEMPLATE 1 Fortilink-C IBF System
35 00846468099510 725-130 725-130 CLARITY II, T-HANDLE DRIVER LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 CLARITY RETRACTOR SYSTEM
36 00846468099480 725-128 725-128 CERVALIGN, Ø2.0MM AWL HWJ AWL 1 CervAlign Anterior Cervical Plate System
37 00846468099411 38-PIN-CADDY 38-PIN-CADDY DOCKING PIN CADDY LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 CLARITY RETRACTOR SYSTEM
38 00846468099404 38-PIN-90 38-PIN-90 DOCKING PIN LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 CLARITY RETRACTOR SYSTEM
39 00846468099398 38-PIN-80 38-PIN-80 DOCKING PIN LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 CLARITY RETRACTOR SYSTEM
40 00846468099381 38-PIN-180 38-PIN-180 DOCKING PIN LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 CLARITY RETRACTOR SYSTEM
41 00846468099374 38-PIN-170 38-PIN-170 DOCKING PIN LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 CLARITY RETRACTOR SYSTEM
42 00846468099367 38-PIN-160 38-PIN-160 DOCKING PIN LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 CLARITY RETRACTOR SYSTEM
43 00846468099350 38-PIN-150 38-PIN-150 DOCKING PIN LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 CLARITY RETRACTOR SYSTEM
44 00846468099343 38-PIN-140 38-PIN-140 DOCKING PIN LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 CLARITY RETRACTOR SYSTEM
45 00846468099336 38-PIN-130 38-PIN-130 DOCKING PIN LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 CLARITY RETRACTOR SYSTEM
46 00846468099329 38-PIN-120 38-PIN-120 DOCKING PIN LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 CLARITY RETRACTOR SYSTEM
47 00846468099312 38-PIN-110 38-PIN-110 DOCKING PIN LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 CLARITY RETRACTOR SYSTEM
48 00846468099305 38-PIN-100 38-PIN-100 DOCKING PIN LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 CLARITY RETRACTOR SYSTEM
49 00846468099299 38-LOCKPIN 38-LOCKPIN DILATOR LOCKING PIN LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 CLARITY RETRACTOR SYSTEM
50 00846468099282 38-180-C-BLD-CADDY 38-180-C-BLD-CADDY 180° CANNULATED BLADE CADDY LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 CLARITY RETRACTOR SYSTEM
Other products with the same Product Code "MAX"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 08806162199499 1108-0810 1108-0810 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
2 08806162124255 1168-0816 1168-0816 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
3 08806162124248 1168-0815 1168-0815 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
4 08806162124231 1168-0814 1168-0814 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
5 08806162124224 1168-0813 1168-0813 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
6 08806162124217 1168-0812 1168-0812 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
7 08806162124200 1168-0811 1168-0811 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
8 08806162124194 1168-0810 1168-0810 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
9 08806162124187 1148-0816 1148-0816 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
10 08806162124170 1148-0815 1148-0815 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
11 08806162124163 1148-0814 1148-0814 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
12 08806162124156 1148-0813 1148-0813 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
13 08806162124149 1148-0812 1148-0812 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
14 08806162124132 1148-0811 1148-0811 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
15 08806162124125 1148-0810 1148-0810 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
16 08806162123951 1168-0416 1168-0416 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
17 08806162123944 1168-0415 1168-0415 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
18 08806162123937 1168-0414 1168-0414 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
19 08806162123920 1168-0413 1168-0413 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
20 08806162123913 1168-0412 1168-0412 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
21 08806162123906 1168-0411 1168-0411 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
22 08806162123890 1168-0410 1168-0410 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
23 08806162123883 1168-0409 1168-0409 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
24 08806162123869 1148-0416 1148-0416 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
25 08806162123852 1148-0415 1148-0415 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
26 08806162123845 1148-0414 1148-0414 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
27 08806162123838 1148-0413 1148-0413 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
28 08806162123821 1148-0412 1148-0412 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
29 08806162123814 1148-0411 1148-0411 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
30 08806162123807 1148-0410 1148-0410 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
31 08806162123791 1148-0409 1148-0409 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
32 08806162123784 1108-0416 1108-0416 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
33 08806162123777 1108-0415 1108-0415 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
34 08806162123760 1108-0414 1108-0414 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
35 08806162123753 1108-0413 1108-0413 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
36 08806162123746 1108-0412 1108-0412 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
37 08806162123739 1108-0411 1108-0411 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
38 08806162123722 1108-0410 1108-0410 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
39 08806162123715 1108-0409 1108-0409 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
40 08806162123500 1108-0015 1108-0015 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
41 08806162121711 1109-1716 1109-1716 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
42 08806162121704 1109-1715 1109-1715 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
43 08806162121698 1109-1714 1109-1714 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
44 08806162121681 1109-1713 1109-1713 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
45 08806162121674 1109-1712 1109-1712 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
46 08806162121667 1109-1711 1109-1711 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
47 08806162121650 1109-1710 1109-1710 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
48 08806162121643 1109-1709 1109-1709 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
49 08806162121636 1109-1708 1109-1708 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
50 08806162121629 1109-1707 1109-1707 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.