Other products from "MEDICAL DESIGNS LLC"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 M364119902FD90 11-9902-FD9 18mm x 21mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedu 18mm x 21mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) and instability in the lumbar spine at one or two contiguous levels from L2 to S1. DDD for lumbar systems is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). The ABC cage devices are used with autogenous bone graft. Patients should be skeletally mature and have had at least six (6) months of non-operative treatment prior to implant. When implanted via a posterior (PLIF, TLIF) approach, this device should be used with supplemental fixation. MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Asfora Bullet Cage® System
2 M364119902FD80 11-9902-FD8 16mm x 25mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedu 16mm x 25mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) and instability in the lumbar spine at one or two contiguous levels from L2 to S1. DDD for lumbar systems is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). The ABC cage devices are used with autogenous bone graft. Patients should be skeletally mature and have had at least six (6) months of non-operative treatment prior to implant. When implanted via a posterior (PLIF, TLIF) approach, this device should be used with supplemental fixation. MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Asfora Bullet Cage® System
3 M364119902FD70 11-9902-FD7 16mm x 21mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedu 16mm x 21mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) and instability in the lumbar spine at one or two contiguous levels from L2 to S1. DDD for lumbar systems is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). The ABC cage devices are used with autogenous bone graft. Patients should be skeletally mature and have had at least six (6) months of non-operative treatment prior to implant. When implanted via a posterior (PLIF, TLIF) approach, this device should be used with supplemental fixation. MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Asfora Bullet Cage® System
4 M364119902FD60 11-9902-FD6 14mm x 25mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedu 14mm x 25mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) and instability in the lumbar spine at one or two contiguous levels from L2 to S1. DDD for lumbar systems is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). The ABC cage devices are used with autogenous bone graft. Patients should be skeletally mature and have had at least six (6) months of non-operative treatment prior to implant. When implanted via a posterior (PLIF, TLIF) approach, this device should be used with supplemental fixation. MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Asfora Bullet Cage® System
5 M364119902FD50 11-9902-FD5 14mm x 21mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedu 14mm x 21mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) and instability in the lumbar spine at one or two contiguous levels from L2 to S1. DDD for lumbar systems is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). The ABC cage devices are used with autogenous bone graft. Patients should be skeletally mature and have had at least six (6) months of non-operative treatment prior to implant. When implanted via a posterior (PLIF, TLIF) approach, this device should be used with supplemental fixation. MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Asfora Bullet Cage® System
6 M364119902FD40 11-9902-FD4 12mm x 25mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedu 12mm x 25mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) and instability in the lumbar spine at one or two contiguous levels from L2 to S1. DDD for lumbar systems is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). The ABC cage devices are used with autogenous bone graft. Patients should be skeletally mature and have had at least six (6) months of non-operative treatment prior to implant. When implanted via a posterior (PLIF, TLIF) approach, this device should be used with supplemental fixation. MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Asfora Bullet Cage® System
7 M364119902FD20 11-9902-FD2 10mm x 25mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedu 10mm x 25mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) and instability in the lumbar spine at one or two contiguous levels from L2 to S1. DDD for lumbar systems is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). The ABC cage devices are used with autogenous bone graft. Patients should be skeletally mature and have had at least six (6) months of non-operative treatment prior to implant. When implanted via a posterior (PLIF, TLIF) approach, this device should be used with supplemental fixation MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Asfora Bullet Cage® System
8 M364119902FD100 11-9902-FD10 18mm x 25mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedu 18mm x 25mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) and instability in the lumbar spine at one or two contiguous levels from L2 to S1. DDD for lumbar systems is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). The ABC cage devices are used with autogenous bone graft. Patients should be skeletally mature and have had at least six (6) months of non-operative treatment prior to implant. When implanted via a posterior (PLIF, TLIF) approach, this device should be used with supplemental fixation. MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Asfora Bullet Cage® System
9 M364119902FD10 11-9902-FD1 10mm x 21mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedu 10mm x 21mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) and instability in the lumbar spine at one or two contiguous levels from L2 to S1. DDD for lumbar systems is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). The ABC cage devices are used with autogenous bone graft. Patients should be skeletally mature and have had at least six (6) months of non-operative treatment prior to implant. When implanted via a posterior (PLIF, TLIF) approach, this device should be used with supplemental fixation. MAX Intervertebral Fusion Device With Bone Graft, Lumbar Asfora Bullet Cage® System
10 M364111109FD920 11-1109-FD9-2 Adjustable Drill Collar OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
11 M364111109FD910 11-1109-FD9-1 Drill Bit OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
12 M364111109FD820 11-1109-FD8-2 Packing Tube OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
13 M364111109FD810 11-1109-FD8-1 Packing Plunger OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
14 M364111109FD730 11-1109-FD7-3 Parallel Guide Sliding Block OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
15 M364111109FD720 11-1109-FD7-2 Parallel Guide Locking Nut OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
16 M364111109FD710 11-1109-FD7-1 Parallel Guide Frame OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
17 M364111109FD211 11-1109-FD21 Long Blunt Steinmann Pin OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone SAMBA SCREW SYSTEM
18 M364111109FD201 11-1109-FD20 Short Blunt Steinmann Pin OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone SAMBA SCREW SYSTEM
19 M364111109FD190 11-1109-FD19 Sterilization Case OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
20 M364111109FD180 11-1109-FD18 Drill Bit T-Handle OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
21 M364111109FD170 11-1109-FD17 Torx Bit T-Handle OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
22 M364111109FD161 11-1109-FD16 Sharp Steinmann Pin OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone SAMBA SCREW SYSTEM
23 M364111109FD150 11-1109-FD15 Plunger Distance Tool OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
24 M364111109FD140 11-1109-FD14 Cannulated Torx Driver Bit OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
25 M364111109FD130 11-1109-FD13 Striker Tube OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
26 M364111109FD110 11-1109-FD11 Pin Sleeve OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
27 M364111109FD100 11-1109-FD10 Drill Guide OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
28 M111109FD120 11-1109-FD12 Drill Gauge HWC,OUR Screw, Fixation, Bone,Sacroiliac Joint Fixation 2 SAMBA SCREW SYSTEM
29 M364111106FD9160 11-1106-FD9-16 16mm Variable Angle Rescue Screw KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
30 M364111106FD9140 11-1106-FD9-14 14mm Variable Angle Rescue Screw KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
31 M364111106FD9120 11-1106-FD9-12 12mm Variable Angle Rescue Screw KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
32 M364111106FD8160 11-1106-FD8-16 16mm Fixed Angle Locking Screw KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
33 M364111106FD8140 11-1106-FD8-14 14mm Fixed Angle Locking Screw KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
34 M364111106FD8120 11-1106-FD8-12 12mm Fixed Angle Locking Screw KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
35 M364111106FD7160 11-1106-FD7-16 16mm Variable Angle Locking Screw KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
36 M364111106FD7140 11-1106-FD7-14 14mm Variable Angle Locking Screw KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
37 M364111106FD7120 11-1106-FD7-12 12mm Variable Angle Locking Screw KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
38 M364111106FD4940 11-1106-FD4-94 4 Level, 94mm Cervical Plate; The Asfora Anterior Cervical Plate System is inten 4 Level, 94mm Cervical Plate; The Asfora Anterior Cervical Plate System is intended to provide temporarystabilization to the anterior spine during the development of cervical spinefusions (C2-T1) for the following indications: degenerative disc disease (DDD)(defined as neck pain of discogenic origin with degeneration of the discconfirmed by history and radiographic studies), spondylolisthesis, trauma (i.e.,fracture or dislocation), spinal stenosis, deformities or curvatures (i.e., scoliosis,kyphosis, and/or lordosis), tumor, pseudoarthrosis, and failed previous fusion. KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
39 M364111106FD4900 11-1106-FD4-90 4 Level, 90mm Cervical Plate; The Asfora Anterior Cervical Plate System is inten 4 Level, 90mm Cervical Plate; The Asfora Anterior Cervical Plate System is intended to provide temporarystabilization to the anterior spine during the development of cervical spinefusions (C2-T1) for the following indications: degenerative disc disease (DDD)(defined as neck pain of discogenic origin with degeneration of the discconfirmed by history and radiographic studies), spondylolisthesis, trauma (i.e.,fracture or dislocation), spinal stenosis, deformities or curvatures (i.e., scoliosis,kyphosis, and/or lordosis), tumor, pseudoarthrosis, and failed previous fusion. KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
40 M364111106FD4860 11-1106-FD4-86 4 Level, 86mm Cervical Plate; The Asfora Anterior Cervical Plate System is inten 4 Level, 86mm Cervical Plate; The Asfora Anterior Cervical Plate System is intended to provide temporarystabilization to the anterior spine during the development of cervical spinefusions (C2-T1) for the following indications: degenerative disc disease (DDD)(defined as neck pain of discogenic origin with degeneration of the discconfirmed by history and radiographic studies), spondylolisthesis, trauma (i.e.,fracture or dislocation), spinal stenosis, deformities or curvatures (i.e., scoliosis,kyphosis, and/or lordosis), tumor, pseudoarthrosis, and failed previous fusion. KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
41 M364111106FD4820 11-1106-FD4-82 4 Level, 82mm Cervical Plate; The Asfora Anterior Cervical Plate System is inten 4 Level, 82mm Cervical Plate; The Asfora Anterior Cervical Plate System is intended to provide temporarystabilization to the anterior spine during the development of cervical spinefusions (C2-T1) for the following indications: degenerative disc disease (DDD)(defined as neck pain of discogenic origin with degeneration of the discconfirmed by history and radiographic studies), spondylolisthesis, trauma (i.e.,fracture or dislocation), spinal stenosis, deformities or curvatures (i.e., scoliosis,kyphosis, and/or lordosis), tumor, pseudoarthrosis, and failed previous fusion. KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
42 M364111106FD4780 11-1106-FD4-78 4 Level, 78mm Cervical Plate; The Asfora Anterior Cervical Plate System is inten 4 Level, 78mm Cervical Plate; The Asfora Anterior Cervical Plate System is intended to provide temporarystabilization to the anterior spine during the development of cervical spinefusions (C2-T1) for the following indications: degenerative disc disease (DDD)(defined as neck pain of discogenic origin with degeneration of the discconfirmed by history and radiographic studies), spondylolisthesis, trauma (i.e.,fracture or dislocation), spinal stenosis, deformities or curvatures (i.e., scoliosis,kyphosis, and/or lordosis), tumor, pseudoarthrosis, and failed previous fusion. KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
43 M364111106FD4740 11-1106-FD4-74 4 Level, 74mm Cervical Plate; The Asfora Anterior Cervical Plate System is inten 4 Level, 74mm Cervical Plate; The Asfora Anterior Cervical Plate System is intended to provide temporarystabilization to the anterior spine during the development of cervical spinefusions (C2-T1) for the following indications: degenerative disc disease (DDD)(defined as neck pain of discogenic origin with degeneration of the discconfirmed by history and radiographic studies), spondylolisthesis, trauma (i.e.,fracture or dislocation), spinal stenosis, deformities or curvatures (i.e., scoliosis,kyphosis, and/or lordosis), tumor, pseudoarthrosis, and failed previous fusion. KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
44 M364111106FD430 11-1106-FD43 Axial Driver Handle KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
45 M364111106FD420 11-1106-FD42 Axial Drill Bit Handle KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
46 M364111106FD410 11-1106-FD41 Fixed Angle Drill Guide KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
47 M364111106FD3750 11-1106-FD3-75 3 Level, 75mm Cervical Plate; The Asfora Anterior Cervical Plate System is inten 3 Level, 75mm Cervical Plate; The Asfora Anterior Cervical Plate System is intended to provide temporarystabilization to the anterior spine during the development of cervical spinefusions (C2-T1) for the following indications: degenerative disc disease (DDD)(defined as neck pain of discogenic origin with degeneration of the discconfirmed by history and radiographic studies), spondylolisthesis, trauma (i.e.,fracture or dislocation), spinal stenosis, deformities or curvatures (i.e., scoliosis,kyphosis, and/or lordosis), tumor, pseudoarthrosis, and failed previous fusion. KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
48 M364111106FD3720 11-1106-FD3-72 3 Level, 72mm Cervical Plate; The Asfora Anterior Cervical Plate System is inten 3 Level, 72mm Cervical Plate; The Asfora Anterior Cervical Plate System is intended to provide temporarystabilization to the anterior spine during the development of cervical spinefusions (C2-T1) for the following indications: degenerative disc disease (DDD)(defined as neck pain of discogenic origin with degeneration of the discconfirmed by history and radiographic studies), spondylolisthesis, trauma (i.e.,fracture or dislocation), spinal stenosis, deformities or curvatures (i.e., scoliosis,kyphosis, and/or lordosis), tumor, pseudoarthrosis, and failed previous fusion. KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
49 M364111106FD370 11-1106-FD37 Sterilization Case KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
50 M364111106FD3690 11-1106-FD3-69 3 Level, 69mm Cervical Plate; The Asfora Anterior Cervical Plate System is inten 3 Level, 69mm Cervical Plate; The Asfora Anterior Cervical Plate System is intended to provide temporarystabilization to the anterior spine during the development of cervical spinefusions (C2-T1) for the following indications: degenerative disc disease (DDD)(defined as neck pain of discogenic origin with degeneration of the discconfirmed by history and radiographic studies), spondylolisthesis, trauma (i.e.,fracture or dislocation), spinal stenosis, deformities or curvatures (i.e., scoliosis,kyphosis, and/or lordosis), tumor, pseudoarthrosis, and failed previous fusion. KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
Other products with the same Product Code "MAX"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 09421028116848 LET30340T LET30340T Intended to be used for the insertion of spinal implants into the spinal space d Intended to be used for the insertion of spinal implants into the spinal space during total artificial disc replacement surgery. CONDUIT LLIF Squid Blade - 26mm ENZTEC LIMITED
2 09421028116831 LET30330T LET30330T Intended to be used for the insertion of spinal implants into the spinal space d Intended to be used for the insertion of spinal implants into the spinal space during total artificial disc replacement surgery. CONDUIT LLIF Squid Blade - 22mm ENZTEC LIMITED
3 09421028116824 LET30320T LET30320T Intended to be used for the insertion of spinal implants into the spinal space d Intended to be used for the insertion of spinal implants into the spinal space during total artificial disc replacement surgery. CONDUIT LLIF Squid Blade - 18mm ENZTEC LIMITED
4 09421028116459 LET30290T LET30290T Intended to be used for the insertion of spinal implants into the spinal space d Intended to be used for the insertion of spinal implants into the spinal space during total artificial disc replacement surgery. CONDUIT LLIF Squid Inserter ENZTEC LIMITED
5 09421028116428 LET30310T LET30310T Intended to be used for the insertion of spinal implants and trials into the spi Intended to be used for the insertion of spinal implants and trials into the spinal space during total artificial disc replacement surgery. CONDUIT LLIF Angled Inserter – Hex Driver ENZTEC LIMITED
6 09421028116411 LET30300T LET30300T Intended to be used for the insertion of spinal implants into the spinal space d Intended to be used for the insertion of spinal implants into the spinal space during total artificial disc replacement surgery. CONDUIT LLIF Angled Implant Inserter ENZTEC LIMITED
7 09421028116404 LET20200T LET20200T Intended to be used for the insertion of spinal trials into the spinal space dur Intended to be used for the insertion of spinal trials into the spinal space during total artificial disc replacement surgery. CONDUIT LLIF Angled Trial Inserter ENZTEC LIMITED
8 09348215026356 PS1-031-127 Arlington PLIF Cage SIGNATURE ORTHOPAEDICS PTY LTD
9 09348215026349 PS1-031-527 Arlington PLIF Cage SIGNATURE ORTHOPAEDICS PTY LTD
10 09348215026332 PS1-031-327 Arlington PLIF Cage SIGNATURE ORTHOPAEDICS PTY LTD
11 09348215026325 PS1-031-227 Arlington PLIF Cage SIGNATURE ORTHOPAEDICS PTY LTD
12 09348215026318 PS1-031-027 Arlington PLIF Cage SIGNATURE ORTHOPAEDICS PTY LTD
13 09348215026301 PS1-031-927 Arlington PLIF Cage SIGNATURE ORTHOPAEDICS PTY LTD
14 09348215026295 PS1-031-727 Arlington PLIF Cage SIGNATURE ORTHOPAEDICS PTY LTD
15 09348215017712 PS1-039-323 Arlington PLIF Cage SIGNATURE ORTHOPAEDICS PTY LTD
16 09348215017705 PS1-039-223 Arlington PLIF Cage SIGNATURE ORTHOPAEDICS PTY LTD
17 09348215017699 PS1-039-123 Arlington PLIF Cage SIGNATURE ORTHOPAEDICS PTY LTD
18 09348215017682 PS1-039-023 Arlington PLIF Cage SIGNATURE ORTHOPAEDICS PTY LTD
19 09348215017675 PS1-039-923 Arlington PLIF Cage SIGNATURE ORTHOPAEDICS PTY LTD
20 09348215017590 PS1-039-527 Arlington PLIF Cage SIGNATURE ORTHOPAEDICS PTY LTD
21 09348215017583 PS1-039-327 Arlington PLIF Cage SIGNATURE ORTHOPAEDICS PTY LTD
22 09348215017576 PS1-039-227 Arlington PLIF Cage SIGNATURE ORTHOPAEDICS PTY LTD
23 09348215017569 PS1-039-127 Arlington PLIF Cage SIGNATURE ORTHOPAEDICS PTY LTD
24 09348215017552 PS1-039-027 Arlington PLIF Cage SIGNATURE ORTHOPAEDICS PTY LTD
25 09348215017545 PS1-039-927 Arlington PLIF Cage SIGNATURE ORTHOPAEDICS PTY LTD
26 09348215017538 PS1-039-727 Arlington PLIF Cage SIGNATURE ORTHOPAEDICS PTY LTD
27 08809596876844 MP82716C Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Po Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Porous matrix, (Angle)8°, (L)27mm, (W)10mm, (H)16mm Medussa-PL Cage MEDYSSEY CO., LTD.
28 08809596876837 MP82715C Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Po Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Porous matrix, (Angle)8°, (L)27mm, (W)10mm, (H)15mm Medussa-PL Cage MEDYSSEY CO., LTD.
29 08809596876820 MP82714C Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Po Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Porous matrix, (Angle)8°, (L)27mm, (W)10mm, (H)14mm Medussa-PL Cage MEDYSSEY CO., LTD.
30 08809596876813 MP82713C Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Po Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Porous matrix, (Angle)8°, (L)27mm, (W)10mm, (H13mm Medussa-PL Cage MEDYSSEY CO., LTD.
31 08809596876806 MP82712C Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Po Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Porous matrix, (Angle)8°, (L)27mm, (W)10mm, (H)12mm Medussa-PL Cage MEDYSSEY CO., LTD.
32 08809596876790 MP82711C Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Po Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Porous matrix, (Angle)8°, (L)27mm, (W)10mm, (H)11mm Medussa-PL Cage MEDYSSEY CO., LTD.
33 08809596876783 MP82710C Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Po Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Porous matrix, (Angle)8°, (L)27mm, (W)10mm, (H)10mm Medussa-PL Cage MEDYSSEY CO., LTD.
34 08809596876776 MP82709C Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Po Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Porous matrix, (Angle)8°, (L)27mm, (W)10mm, (H)9mm Medussa-PL Cage MEDYSSEY CO., LTD.
35 08809596876769 MP82708C Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Po Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Porous matrix, (Angle)8°, (L)27mm, (W)10mm, (H)8mm Medussa-PL Cage MEDYSSEY CO., LTD.
36 08809596876752 MP82516C Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Po Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Porous matrix, (Angle)8°, (L)25mm, (W)10mm, (H)16mm Medussa-PL Cage MEDYSSEY CO., LTD.
37 08809596876745 MP82515C Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Po Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Porous matrix, (Angle)8°, (L)25mm, (W)10mm, (H)15mm Medussa-PL Cage MEDYSSEY CO., LTD.
38 08809596876738 MP82514C Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Po Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Porous matrix, (Angle)8°, (L)25mm, (W)10mm, (H)14mm Medussa-PL Cage MEDYSSEY CO., LTD.
39 08809596876721 MP82513C Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Po Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Porous matrix, (Angle)8°, (L)25mm, (W)10mm, (H13mm Medussa-PL Cage MEDYSSEY CO., LTD.
40 08809596876714 MP82512C Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Po Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Porous matrix, (Angle)8°, (L)25mm, (W)10mm, (H)12mm Medussa-PL Cage MEDYSSEY CO., LTD.
41 08809596876707 MP82511C Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Po Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Porous matrix, (Angle)8°, (L)25mm, (W)10mm, (H)11mm Medussa-PL Cage MEDYSSEY CO., LTD.
42 08809596876691 MP82510C Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Po Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Porous matrix, (Angle)8°, (L)25mm, (W)10mm, (H)10mm Medussa-PL Cage MEDYSSEY CO., LTD.
43 08809596876684 MP82509C Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Po Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Porous matrix, (Angle)8°, (L)25mm, (W)10mm, (H)9mm Medussa-PL Cage MEDYSSEY CO., LTD.
44 08809596876677 MP82508C Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Po Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Porous matrix, (Angle)8°, (L)25mm, (W)10mm, (H)8mm Medussa-PL Cage MEDYSSEY CO., LTD.
45 08809596876660 MP42716C Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Po Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Porous matrix, (Angle)4°, (L)27mm, (W)10mm, (H)16mm Medussa-PL Cage MEDYSSEY CO., LTD.
46 08809596876653 MP42715C Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Po Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Porous matrix, (Angle)4°, (L)27mm, (W)10mm, (H)15mm Medussa-PL Cage MEDYSSEY CO., LTD.
47 08809596876646 MP42714C Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Po Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Porous matrix, (Angle)4°, (L)27mm, (W)10mm, (H)14mm Medussa-PL Cage MEDYSSEY CO., LTD.
48 08809596876639 MP42713C Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Po Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Porous matrix, (Angle)4°, (L)27mm, (W)10mm, (H13mm Medussa-PL Cage MEDYSSEY CO., LTD.
49 08809596876622 MP42712C Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Po Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Porous matrix, (Angle)4°, (L)27mm, (W)10mm, (H)12mm Medussa-PL Cage MEDYSSEY CO., LTD.
50 08809596876615 MP42711C Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Po Medussa-PL Cage, Non-sterile type, Posterior lumbar interbody fusion cage, 3D Porous matrix, (Angle)4°, (L)27mm, (W)10mm, (H)11mm Medussa-PL Cage MEDYSSEY CO., LTD.