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 M364119902FD30 11-9902-FD3 12mm x 21mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedu 12mm 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
8 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
9 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
10 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
11 M364111109FD920 11-1109-FD9-2 Adjustable Drill Collar OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
12 M364111109FD910 11-1109-FD9-1 Drill Bit OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
13 M364111109FD820 11-1109-FD8-2 Packing Tube OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
14 M364111109FD810 11-1109-FD8-1 Packing Plunger OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
15 M364111109FD730 11-1109-FD7-3 Parallel Guide Sliding Block OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
16 M364111109FD720 11-1109-FD7-2 Parallel Guide Locking Nut OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
17 M364111109FD710 11-1109-FD7-1 Parallel Guide Frame OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
18 M364111109FD211 11-1109-FD21 Long Blunt Steinmann Pin OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone SAMBA SCREW SYSTEM
19 M364111109FD201 11-1109-FD20 Short Blunt Steinmann Pin OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone SAMBA SCREW SYSTEM
20 M364111109FD190 11-1109-FD19 Sterilization Case OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
21 M364111109FD180 11-1109-FD18 Drill Bit T-Handle OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
22 M364111109FD170 11-1109-FD17 Torx Bit T-Handle OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 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 Codes "OUR, HWC"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 10603295007708 1172-70-000 117270000 CANCELLOUS BONE SCREW 6.5mm x 70mm NA DEPUY ORTHOPAEDICS, INC.
2 10603295007692 1172-65-000 117265000 CANCELLOUS BONE SCREW 6.5mm x 65mm NA DEPUY ORTHOPAEDICS, INC.
3 10603295007685 1172-60-000 117260000 CANCELLOUS BONE SCREW 6.5mm x 60mm NA DEPUY ORTHOPAEDICS, INC.
4 10603295007678 1172-55-000 117255000 CANCELLOUS BONE SCREW 6.5mm x 55mm NA DEPUY ORTHOPAEDICS, INC.
5 10603295007661 1172-50-000 117250000 CANCELLOUS BONE SCREW 6.5mm x 50mm NA DEPUY ORTHOPAEDICS, INC.
6 10603295007654 1172-45-000 117245000 CANCELLOUS BONE SCREW 6.5mm x 45mm NA DEPUY ORTHOPAEDICS, INC.
7 10603295007647 1172-40-000 117240000 CANCELLOUS BONE SCREW 6.5mm x 40mm NA DEPUY ORTHOPAEDICS, INC.
8 10603295007630 1172-35-000 117235000 CANCELLOUS BONE SCREW 6.5mm x 35mm NA DEPUY ORTHOPAEDICS, INC.
9 10603295007623 1172-30-000 117230000 CANCELLOUS BONE SCREW 6.5mm x 30mm NA DEPUY ORTHOPAEDICS, INC.
10 10603295007616 1172-25-000 117225000 CANCELLOUS BONE SCREW 6.5mm x 25mm NA DEPUY ORTHOPAEDICS, INC.
11 10603295007609 1172-20-000 117220000 CANCELLOUS BONE SCREW 6.5mm x 20mm NA DEPUY ORTHOPAEDICS, INC.
12 10603295007593 1172-15-000 117215000 CANCELLOUS BONE SCREW 6.5mm x 15mm NA DEPUY ORTHOPAEDICS, INC.
13 10381780441380 MBAIMP MBAIMP MBA Implant Set MBA™ Titanium Subtalar Implant System ASCENSION ORTHOPEDICS, INC.
14 10381780257288 MBASET MBA™ Instrument Set (05-5000) MBA™ ASCENSION ORTHOPEDICS, INC.
15 10381780257271 KOMPSET Kompressor™ Instrument Set (21-5000) Kompressor™ ASCENSION ORTHOPEDICS, INC.
16 10381780237686 TRL-1006-C06 The Integra Titanium Bone Wedges are a series of wedge-shaped devices intended t The Integra Titanium Bone Wedges are a series of wedge-shaped devices intended to be used for angular correction of small bones in the ankle and foot. The Integra Titanium Bone Wedges are constructed from commercially pure titanium formed into a cancellous-like structure. Trial Cotton 20 X 6.5 TiWedge™ ASCENSION ORTHOPEDICS, INC.
17 10381780237679 TRL-1006-C05 The Integra® Titanium Cotton Wedge Trials are inserted until the footprint is co The Integra® Titanium Cotton Wedge Trials are inserted until the footprint is congruent to the dimensions of the osteotomy surface, and the desired amount of correction is achieved. The trial is to confirm that the implanted wedge will be congruent with the osteotomy surface to provide the most optimal site for ingrowth of bone into the wedge. TiWedge™ ASCENSION ORTHOPEDICS, INC.
18 10381780237662 TRL-1006-C04 The Integra® Titanium Cotton Wedge Trials are inserted until the footprint is co The Integra® Titanium Cotton Wedge Trials are inserted until the footprint is congruent to the dimensions of the osteotomy surface, and the desired amount of correction is achieved. The trial is to confirm that the implanted wedge will be congruent with the osteotomy surface to provide the most optimal site for ingrowth of bone into the wedge. TiWedge™ ASCENSION ORTHOPEDICS, INC.
19 10381780237655 TRL-1006-C03 The Integra® Titanium Cotton Wedge Trials are inserted until the footprint is co The Integra® Titanium Cotton Wedge Trials are inserted until the footprint is congruent to the dimensions of the osteotomy surface, and the desired amount of correction is achieved. The trial is to confirm that the implanted wedge will be congruent with the osteotomy surface to provide the most optimal site for ingrowth of bone into the wedge. TiWedge™ ASCENSION ORTHOPEDICS, INC.
20 10381780237648 TRL-1006-C02 The Integra® Titanium Cotton Wedge Trials are inserted until the footprint is co The Integra® Titanium Cotton Wedge Trials are inserted until the footprint is congruent to the dimensions of the osteotomy surface, and the desired amount of correction is achieved. The trial is to confirm that the implanted wedge will be congruent with the osteotomy surface to provide the most optimal site for ingrowth of bone into the wedge. TiWedge™ ASCENSION ORTHOPEDICS, INC.
21 10381780237631 TRL-1006-C01 The Integra® Titanium Cotton Wedge Trials are inserted until the footprint is co The Integra® Titanium Cotton Wedge Trials are inserted until the footprint is congruent to the dimensions of the osteotomy surface, and the desired amount of correction is achieved. The trial is to confirm that the implanted wedge will be congruent with the osteotomy surface to provide the most optimal site for ingrowth of bone into the wedge. TiWedge™ ASCENSION ORTHOPEDICS, INC.
22 10381780237624 TRL-1006-L09 The Integra® Titanium Bone WedgeTrials are inserted until the footprint is congr The Integra® Titanium Bone WedgeTrials are inserted until the footprint is congruent to the dimensions of the osteotomy surface, and the desired amount of correction is achieved. The trial is to confirm that the implanted wedge will be congruent with the osteotomy surface to provide the most optimal site for ingrowth of bone into the wedge. TiWedge™ ASCENSION ORTHOPEDICS, INC.
23 10381780237617 TRL-1006-L08 The Integra® Titanium Bone WedgeTrials are inserted until the footprint is congr The Integra® Titanium Bone WedgeTrials are inserted until the footprint is congruent to the dimensions of the osteotomy surface, and the desired amount of correction is achieved. The trial is to confirm that the implanted wedge will be congruent with the osteotomy surface to provide the most optimal site for ingrowth of bone into the wedge. TiWedge™ ASCENSION ORTHOPEDICS, INC.
24 10381780237600 TRL-1006-L07 The Integra® Titanium Bone WedgeTrials are inserted until the footprint is congr The Integra® Titanium Bone WedgeTrials are inserted until the footprint is congruent to the dimensions of the osteotomy surface, and the desired amount of correction is achieved. The trial is to confirm that the implanted wedge will be congruent with the osteotomy surface to provide the most optimal site for ingrowth of bone into the wedge. TiWedge™ ASCENSION ORTHOPEDICS, INC.
25 10381780237594 TRL-1006-L06 The Integra® Titanium Bone WedgeTrials are inserted until the footprint is congr The Integra® Titanium Bone WedgeTrials are inserted until the footprint is congruent to the dimensions of the osteotomy surface, and the desired amount of correction is achieved. The trial is to confirm that the implanted wedge will be congruent with the osteotomy surface to provide the most optimal site for ingrowth of bone into the wedge. TiWedge™ ASCENSION ORTHOPEDICS, INC.
26 10381780237587 TRL-1006-L05 The Integra® Titanium Bone WedgeTrials are inserted until the footprint is congr The Integra® Titanium Bone WedgeTrials are inserted until the footprint is congruent to the dimensions of the osteotomy surface, and the desired amount of correction is achieved. The trial is to confirm that the implanted wedge will be congruent with the osteotomy surface to provide the most optimal site for ingrowth of bone into the wedge. TiWedge™ ASCENSION ORTHOPEDICS, INC.
27 10381780237570 TRL-1006-L04 The Integra® Titanium Bone WedgeTrials are inserted until the footprint is congr The Integra® Titanium Bone WedgeTrials are inserted until the footprint is congruent to the dimensions of the osteotomy surface, and the desired amount of correction is achieved. The trial is to confirm that the implanted wedge will be congruent with the osteotomy surface to provide the most optimal site for ingrowth of bone into the wedge. TiWedge™ ASCENSION ORTHOPEDICS, INC.
28 10381780237563 TRL-1006-L03 The Integra® Titanium Bone WedgeTrials are inserted until the footprint is congr The Integra® Titanium Bone WedgeTrials are inserted until the footprint is congruent to the dimensions of the osteotomy surface, and the desired amount of correction is achieved. The trial is to confirm that the implanted wedge will be congruent with the osteotomy surface to provide the most optimal site for ingrowth of bone into the wedge. TiWedge™ ASCENSION ORTHOPEDICS, INC.
29 10381780237556 TRL-1006-L02 The Integra® Titanium Bone WedgeTrials are inserted until the footprint is congr The Integra® Titanium Bone WedgeTrials are inserted until the footprint is congruent to the dimensions of the osteotomy surface, and the desired amount of correction is achieved. The trial is to confirm that the implanted wedge will be congruent with the osteotomy surface to provide the most optimal site for ingrowth of bone into the wedge. TiWedge™ ASCENSION ORTHOPEDICS, INC.
30 10381780237549 TRL-1006-L01 The Integra® Titanium Bone WedgeTrials are inserted until the footprint is congr The Integra® Titanium Bone WedgeTrials are inserted until the footprint is congruent to the dimensions of the osteotomy surface, and the desired amount of correction is achieved. The trial is to confirm that the implanted wedge will be congruent with the osteotomy surface to provide the most optimal site for ingrowth of bone into the wedge. TiWedge™ ASCENSION ORTHOPEDICS, INC.
31 10381780237471 TIWEDGEINSTP The Integra Titanium Bone Wedge is intended to be used for internal bone fixatio The Integra Titanium Bone Wedge is intended to be used for internal bone fixation for bone fractures or osteotomies in the ankle and foot. This set includes LCL trials and cotton trials to evaluate proper size and fit of the implants. A wedge inserter and tamp are also included for assistance. TiWedgeTM ASCENSION ORTHOPEDICS, INC.
32 10381780124948 TBW-1006-2065 TBW-1006-2065 The Integra® Titanium Bone Wedges are intended to be used for internal bone fixa The Integra® Titanium Bone Wedges are intended to be used for internal bone fixation for bone fracturesor osteotomies in the ankle and foot Integra® Titanium Bone Wedge System ASCENSION ORTHOPEDICS, INC.
33 10381780124931 TBW-1006-2055 TBW-1006-2055 The Integra® Titanium Bone Wedges are intended to be used for internal bone fixa The Integra® Titanium Bone Wedges are intended to be used for internal bone fixation for bone fracturesor osteotomies in the ankle and foot Integra® Titanium Bone Wedge System ASCENSION ORTHOPEDICS, INC.
34 10381780124924 TBW-1006-2045 TBW-1006-2045 The Integra® Titanium Bone Wedges are intended to be used for internal bone fixa The Integra® Titanium Bone Wedges are intended to be used for internal bone fixation for bone fracturesor osteotomies in the ankle and foot Integra® Titanium Bone Wedge System ASCENSION ORTHOPEDICS, INC.
35 10381780124917 TBW-1006-1665 TBW-1006-1665 The Integra® Titanium Bone Wedges are intended to be used for internal bone fixa The Integra® Titanium Bone Wedges are intended to be used for internal bone fixation for bone fracturesor osteotomies in the ankle and foot Integra® Titanium Bone Wedge System ASCENSION ORTHOPEDICS, INC.
36 10381780124900 TBW-1006-1655 TBW-1006-1655 The Integra® Titanium Bone Wedges are intended to be used for internal bone fixa The Integra® Titanium Bone Wedges are intended to be used for internal bone fixation for bone fracturesor osteotomies in the ankle and foot Integra® Titanium Bone Wedge System ASCENSION ORTHOPEDICS, INC.
37 10381780124894 TBW-1006-1645 TBW-1006-1645 The Integra® Titanium Bone Wedges are intended to be used for internal bone fixa The Integra® Titanium Bone Wedges are intended to be used for internal bone fixation for bone fracturesor osteotomies in the ankle and foot Integra® Titanium Bone Wedge System ASCENSION ORTHOPEDICS, INC.
38 10381780124887 TBW-1006-LG12 TBW-1006-LG12 The Integra® Titanium Bone Wedges are intended to be used for internal bone fixa The Integra® Titanium Bone Wedges are intended to be used for internal bone fixation for bone fracturesor osteotomies in the ankle and foot Integra® Titanium Bone Wedge System ASCENSION ORTHOPEDICS, INC.
39 10381780124870 TBW-1006-LG10 TBW-1006-LG10 The Integra® Titanium Bone Wedges are intended to be used for internal bone fixa The Integra® Titanium Bone Wedges are intended to be used for internal bone fixation for bone fracturesor osteotomies in the ankle and foot Integra® Titanium Bone Wedge System ASCENSION ORTHOPEDICS, INC.
40 10381780124863 TBW-1006-LG8 TBW-1006-LG8 The Integra® Titanium Bone Wedges are intended to be used for internal bone fixa The Integra® Titanium Bone Wedges are intended to be used for internal bone fixation for bone fracturesor osteotomies in the ankle and foot Integra® Titanium Bone Wedge System ASCENSION ORTHOPEDICS, INC.
41 10381780124856 TBW-1006-MD12 TBW-1006-MD12 The Integra® Titanium Bone Wedges are intended to be used for internal bone fixa The Integra® Titanium Bone Wedges are intended to be used for internal bone fixation for bone fracturesor osteotomies in the ankle and foot Integra® Titanium Bone Wedge System ASCENSION ORTHOPEDICS, INC.
42 10381780124849 TBW-1006-MD10 TBW-1006-MD10 The Integra® Titanium Bone Wedges are intended to be used for internal bone fixa The Integra® Titanium Bone Wedges are intended to be used for internal bone fixation for bone fracturesor osteotomies in the ankle and foot Integra® Titanium Bone Wedge System ASCENSION ORTHOPEDICS, INC.
43 10381780124832 TBW-1006-MD8 TBW-1006-MD8 The Integra® Titanium Bone Wedges are intended to be used for internal bone fixa The Integra® Titanium Bone Wedges are intended to be used for internal bone fixation for bone fracturesor osteotomies in the ankle and foot Integra® Titanium Bone Wedge System ASCENSION ORTHOPEDICS, INC.
44 10381780124825 TBW-1006-SM12 TBW-1006-SM12 The Integra® Titanium Bone Wedges are intended to be used for internal bone fixa The Integra® Titanium Bone Wedges are intended to be used for internal bone fixation for bone fracturesor osteotomies in the ankle and foot Integra® Titanium Bone Wedge System ASCENSION ORTHOPEDICS, INC.
45 10381780124818 TBW-1006-SM10 TBW-1006-SM10 The Integra® Titanium Bone Wedges are intended to be used for internal bone fixa The Integra® Titanium Bone Wedges are intended to be used for internal bone fixation for bone fracturesor osteotomies in the ankle and foot Integra® Titanium Bone Wedge System ASCENSION ORTHOPEDICS, INC.
46 10381780124801 TBW-1006-SM8 TBW-1006-SM8 The Integra® Titanium Bone Wedges are intended to be used for internal bone fixa The Integra® Titanium Bone Wedges are intended to be used for internal bone fixation for bone fracturesor osteotomies in the ankle and foot Integra® Titanium Bone Wedge System ASCENSION ORTHOPEDICS, INC.
47 10381780123064 CSS500000670WT CSS500000670WT The washer is used in conjunction with the Capture High Torque Screw System. CAPTURE™ High Torque Screw System ASCENSION ORTHOPEDICS, INC.
48 10381780123057 CSS500000650WT CSS500000650WT The washer is used in conjunction with the Capture High Torque Screw System. CAPTURE™ High Torque Screw System ASCENSION ORTHOPEDICS, INC.
49 10381780123040 CSS500000640WT CSS500000640WT The washer is used in conjunction with the Capture High Torque Screw System. CAPTURE™ High Torque Screw System ASCENSION ORTHOPEDICS, INC.
50 10381780123033 CSS500000630WT CSS500000630WT The washer is used in conjunction with the Capture High Torque Screw System. CAPTURE™ High Torque Screw System ASCENSION ORTHOPEDICS, INC.