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 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
3 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
4 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
5 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
6 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
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 00857215007153 10250800 10250800 THE AUDERE POSTERIOR LUMBAR SPACER SYSTEM CONSISTS OF IMPLANTS, TRIALS AND INSTR THE AUDERE POSTERIOR LUMBAR SPACER SYSTEM CONSISTS OF IMPLANTS, TRIALS AND INSTRUMENTS. THE AUDERE LUMBAR SPACER SYSTEM MAY BE IMPLANTED BILATERALLY USING A POSTERIOR (PLIF) APPROACH, OR AS A SINGLE DEVICE EMPLOYING A TRANSFORAMINAL (TLIF) APPROACH. AUDERE POSTERIOR LUMBAR SPACER SYSTEM MET 1 TECHNOLOGIES, LLC
2 00857215007146 10250700 10250700 THE AUDERE POSTERIOR LUMBAR SPACER SYSTEM CONSISTS OF IMPLANTS, TRIALS AND INSTR THE AUDERE POSTERIOR LUMBAR SPACER SYSTEM CONSISTS OF IMPLANTS, TRIALS AND INSTRUMENTS. THE AUDERE LUMBAR SPACER SYSTEM MAY BE IMPLANTED BILATERALLY USING A POSTERIOR (PLIF) APPROACH, OR AS A SINGLE DEVICE EMPLOYING A TRANSFORAMINAL (TLIF) APPROACH. AUDERE POSTERIOR LUMBAR SPACER SYSTEM MET 1 TECHNOLOGIES, LLC
3 00857215007139 10201400 10201400 THE AUDERE POSTERIOR LUMBAR SPACER SYSTEM CONSISTS OF IMPLANTS, TRIALS AND INSTR THE AUDERE POSTERIOR LUMBAR SPACER SYSTEM CONSISTS OF IMPLANTS, TRIALS AND INSTRUMENTS. THE AUDERE LUMBAR SPACER SYSTEM MAY BE IMPLANTED BILATERALLY USING A POSTERIOR (PLIF) APPROACH, OR AS A SINGLE DEVICE EMPLOYING A TRANSFORAMINAL (TLIF) APPROACH. AUDERE POSTERIOR LUMBAR SPACER SYSTEM MET 1 TECHNOLOGIES, LLC
4 00857215007122 10201300 10201300 THE AUDERE POSTERIOR LUMBAR SPACER SYSTEM CONSISTS OF IMPLANTS, TRIALS AND INSTR THE AUDERE POSTERIOR LUMBAR SPACER SYSTEM CONSISTS OF IMPLANTS, TRIALS AND INSTRUMENTS. THE AUDERE LUMBAR SPACER SYSTEM MAY BE IMPLANTED BILATERALLY USING A POSTERIOR (PLIF) APPROACH, OR AS A SINGLE DEVICE EMPLOYING A TRANSFORAMINAL (TLIF) APPROACH. AUDERE POSTERIOR LUMBAR SPACER SYSTEM MET 1 TECHNOLOGIES, LLC
5 00857215007115 10201200 10201200 The AUDERE Posterior Lumbar Spacer System consists of implants, trials and instr The AUDERE Posterior Lumbar Spacer System consists of implants, trials and instruments. The AUDERE Lumbar Spacer System may be implanted bilaterally using a posterior (PLIF) approach, or as a single device employing a transforaminal (TLIF) approach. AUDERE POSTERIOR LUMBAR SPACER SYSTEM MET 1 TECHNOLOGIES, LLC
6 00857215007108 10201100 10201100 The AUDERE Posterior Lumbar Spacer System consists of implants, trials and instr The AUDERE Posterior Lumbar Spacer System consists of implants, trials and instruments. The AUDERE Lumbar Spacer System may be implanted bilaterally using a posterior (PLIF) approach, or as a single device employing a transforaminal (TLIF) approach. AUDERE POSTERIOR LUMBAR SPACER SYSTEM MET 1 TECHNOLOGIES, LLC
7 00857215007092 10201000 10201000 THE AUDERE POSTERIOR LUMBAR SPACER SYSTEM CONSISTS OF IMPLANTS, TRIALS AND INSTR THE AUDERE POSTERIOR LUMBAR SPACER SYSTEM CONSISTS OF IMPLANTS, TRIALS AND INSTRUMENTS. THE AUDERE LUMBAR SPACER SYSTEM MAY BE IMPLANTED BILATERALLY USING A POSTERIOR (PLIF) APPROACH, OR AS A SINGLE DEVICE EMPLOYING A TRANSFORAMINAL (TLIF) APPROACH. AUDERE POSTERIOR LUMBAR SPACER SYSTEM MET 1 TECHNOLOGIES, LLC
8 00857215007085 10200900 10200900 The AUDERE Posterior Lumbar Spacer System consists of implants, trials and instr The AUDERE Posterior Lumbar Spacer System consists of implants, trials and instruments. TheAUDERE Lumbar Spacer System may be implanted bilaterally using a posterior (PLIF) approach,or as a single device employing a transforaminal (TLIF) approach. AUDERE POSTERIOR LUMBAR SPACER SYSTEM MET 1 TECHNOLOGIES, LLC
9 00857215007078 10200800 10200800 THE AUDERE POSTERIOR LUMBAR SPACER SYSTEM CONSISTS OF IMPLANTS, TRIALS AND INSTR THE AUDERE POSTERIOR LUMBAR SPACER SYSTEM CONSISTS OF IMPLANTS, TRIALS AND INSTRUMENTS. THE AUDERE LUMBAR SPACER SYSTEM MAY BE IMPLANTED BILATERALLY USING A POSTERIOR (PLIF) APPROACH, OR AS A SINGLE DEVICE EMPLOYING A TRANSFORAMINAL (TLIF) APPROACH. AUDERE POSTERIOR LUMBAR SPACER SYSTEM MET 1 TECHNOLOGIES, LLC
10 00857215007061 10200700 10200700 THE AUDERE POSTERIOR LUMBAR SPACER SYSTEM CONSISTS OF IMPLANTS, TRIALS AND INSTR THE AUDERE POSTERIOR LUMBAR SPACER SYSTEM CONSISTS OF IMPLANTS, TRIALS AND INSTRUMENTS. THE AUDERE LUMBAR SPACER SYSTEM MAY BE IMPLANTED BILATERALLY USING A POSTERIOR (PLIF) APPROACH, OR AS A SINGLE DEVICE EMPLOYING A TRANSFORAMINAL (TLIF) APPROACH. AUDERE POSTERIOR LUMBAR SPACER SYSTEM MET 1 TECHNOLOGIES, LLC
11 00857215007054 10251400 10251400 THE AUDERE POSTERIOR LUMBAR SPACER SYSTEM CONSISTS OF IMPLANTS, TRIALS AND INSTR THE AUDERE POSTERIOR LUMBAR SPACER SYSTEM CONSISTS OF IMPLANTS, TRIALS AND INSTRUMENTS. THE AUDERE LUMBAR SPACER SYSTEM MAY BE IMPLANTED BILATERALLY USING A POSTERIOR (PLIF) APPROACH, OR AS A SINGLE DEVICE EMPLOYING A TRANSFORAMINAL (TLIF) APPROACH. AUDERE POSTERIOR LUMBAR SPACER SYSTEM MET 1 TECHNOLOGIES, LLC
12 00857215007047 10251300 10251300 THE AUDERE POSTERIOR LUMBAR SPACER SYSTEM CONSISTS OF IMPLANTS, TRIALS AND INSTR THE AUDERE POSTERIOR LUMBAR SPACER SYSTEM CONSISTS OF IMPLANTS, TRIALS AND INSTRUMENTS. THE AUDERE LUMBAR SPACER SYSTEM MAY BE IMPLANTED BILATERALLY USING A POSTERIOR (PLIF) APPROACH, OR AS A SINGLE DEVICE EMPLOYING A TRANSFORAMINAL (TLIF) APPROACH. AUDERE POSTERIOR LUMBAR SPACER SYSTEM MET 1 TECHNOLOGIES, LLC
13 00857215007030 10251200 10251200 THE AUDERE POSTERIOR LUMBAR SPACER SYSTEM CONSISTS OF IMPLANTS, TRIALS AND INSTR THE AUDERE POSTERIOR LUMBAR SPACER SYSTEM CONSISTS OF IMPLANTS, TRIALS AND INSTRUMENTS. THE AUDERE LUMBAR SPACER SYSTEM MAY BE IMPLANTED BILATERALLY USING A POSTERIOR (PLIF) APPROACH, OR AS A SINGLE DEVICE EMPLOYING A TRANSFORAMINAL (TLIF) APPROACH. AUDERE POSTERIOR LUMBAR SPACER SYSTEM MET 1 TECHNOLOGIES, LLC
14 00857215007023 10251100 10251100 THE AUDERE POSTERIOR LUMBAR SPACER SYSTEM CONSISTS OF IMPLANTS, TRIALS AND INSTR THE AUDERE POSTERIOR LUMBAR SPACER SYSTEM CONSISTS OF IMPLANTS, TRIALS AND INSTRUMENTS. THE AUDERE LUMBAR SPACER SYSTEM MAY BE IMPLANTED BILATERALLY USING A POSTERIOR (PLIF) APPROACH, OR AS A SINGLE DEVICE EMPLOYING A TRANSFORAMINAL (TLIF) APPROACH. AUDERE POSTERIOR LUMBAR SPACER SYSTEM MET 1 TECHNOLOGIES, LLC
15 00857215007016 10251000 10251000 THE AUDERE POSTERIOR LUMBAR SPACER SYSTEM CONSISTS OF IMPLANTS, TRIALS AND INSTR THE AUDERE POSTERIOR LUMBAR SPACER SYSTEM CONSISTS OF IMPLANTS, TRIALS AND INSTRUMENTS. THE AUDERE LUMBAR SPACER SYSTEM MAY BE IMPLANTED BILATERALLY USING A POSTERIOR (PLIF) APPROACH, OR AS A SINGLE DEVICE EMPLOYING A TRANSFORAMINAL (TLIF) APPROACH. AUDERE POSTERIOR LUMBAR SPACER SYSTEM MET 1 TECHNOLOGIES, LLC
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18 00856037005811 PPT-P268010-S PPT-P268010-S TiLink-P - 26mm x 10mm x 8mm x 0° TiLink-P TYBER MEDICAL LLC
19 00856037005804 PPT-P2612010-S PPT-P2612010-S TiLink-P - 26mm x 10mm x 12mm x 0° TiLink-P TYBER MEDICAL LLC
20 00856037005798 PPT-P2611010-S PPT-P2611010-S TiLink-P - 26mm x 10mm x 11mm x 0° TiLink-P TYBER MEDICAL LLC
21 00856037005781 PPT-P2610010-S PPT-P2610010-S TiLink-P - 26mm x 10mm x 10mm x 0° TiLink-P TYBER MEDICAL LLC
22 00856037005316 21-34100515 21-34100515 TiLink-T - 34mm x 10mm x 15mm x 5 deg TiLink-T TYBER MEDICAL LLC
23 00856037005309 21-34100513 21-34100513 TiLink-T - 34mm x 10mm x 13mm x 5 deg TiLink-T TYBER MEDICAL LLC
24 00856037005293 21-34100512 21-34100512 TiLink-T - 34mm x 10mm x 12mm x 5 deg TiLink-T TYBER MEDICAL LLC
25 00856037005286 21-34100511 21-34100511 TiLink-T - 34mm x 10mm x 11mm x 5 deg TiLink-T TYBER MEDICAL LLC
26 00856037005279 21-34100510 21-34100510 TiLink-T - 34mm x 10mm x 10mm x 5 deg TiLink-T TYBER MEDICAL LLC
27 00856037005262 21-34100509 21-34100509 TiLink-T - 34mm x 10mm x 9mm x 5 deg TiLink-T TYBER MEDICAL LLC
28 00856037005255 21-34100508 21-34100508 TiLink-T - 34mm x 10mm x 8mm x 5 deg TiLink-T TYBER MEDICAL LLC
29 00856037005248 21-34100507 21-34100507 TiLink-T - 34mm x 10mm x 7mm x 5 deg TiLink-T TYBER MEDICAL LLC
30 00856037005231 21-30100515 21-30100515 TiLink-T 30mm x 10mm x 15mm x 5 deg TiLink-T TYBER MEDICAL LLC
31 00856037005224 21-30100513 21-30100513 TiLink-T 30mm x 10mm x 13mm x 5 deg TiLink-T TYBER MEDICAL LLC
32 00856037005217 21-30100512 21-30100512 TiLink-T 30mm x 10mm x 12mm x 5 deg TiLink-T TYBER MEDICAL LLC
33 00856037005200 21-30100511 21-30100511 TiLink-T 30mm x 10mm x 11mm x 5 deg TiLink-T TYBER MEDICAL LLC
34 00856037005194 21-30100510 21-30100510 TiLink-T 30mm x 10mm x 10mm x 5 deg TiLink-T TYBER MEDICAL LLC
35 00856037005187 21-30100509 21-30100509 TiLink-T 30mm x 10mm x 9mm x 5 deg TiLink-T TYBER MEDICAL LLC
36 00856037005170 21-30100508 21-30100508 TiLink-T 30mm x 10mm x 8mm x 5 deg TiLink-T TYBER MEDICAL LLC
37 00856037005163 21-30100507 21-30100507 TiLink-T 30mm x 10mm x 7mm x 5 deg TiLink-T TYBER MEDICAL LLC
38 00856037005156 20-26100815 20-26100815 TiLink-P 26mm x 10mm x 15mm x 8 deg TiLink-P TYBER MEDICAL LLC
39 00856037005149 20-26100813 20-26100813 TiLink-P 26mm x 10mm x 13mm x 8 deg TiLink-P TYBER MEDICAL LLC
40 00856037005132 20-26100812 20-26100812 TiLink-P 26mm x 10mm x 12mm x 8 deg TiLink-P TYBER MEDICAL LLC
41 00856037005101 20-26100809 20-26100809 TiLink-P 26mm x 10mm x 9mm x 8 deg TiLink-P TYBER MEDICAL LLC
42 00856037005095 20-26100808 20-26100808 TiLink-P 26mm x 10mm x 8mm x 8 deg TiLink-P TYBER MEDICAL LLC
43 00856037005088 20-26100807 20-26100807 TiLink-P 26mm x 10mm x 7mm x 8 deg TiLink-P TYBER MEDICAL LLC
44 00856037005071 30-14120512 30-14120512 TiLink-C 14mm x 12mm x 5 deg Curved TiLink-C TYBER MEDICAL LLC
45 00856037005064 30-14120511 30-14120511 TiLink-C 14mm x 11mm x 5 deg Curved TiLink-C TYBER MEDICAL LLC
46 00856037005057 30-14120510 30-14120510 TiLink-C 14mm x 10mm x 5 deg Curved TiLink-C TYBER MEDICAL LLC
47 00856037005040 30-14120509 30-14120509 TiLink-C 14mm x 9mm x 5 deg Curved TiLink-C TYBER MEDICAL LLC
48 00856037005033 30-14120508 30-14120508 TiLink-C 14mm x 8mm x 5 deg Curved TiLink-C TYBER MEDICAL LLC
49 00856037005026 30-14120507 30-14120507 TiLink-C 14mm x 7mm x 5 deg Curved TiLink-C TYBER MEDICAL LLC
50 00856037005019 30-14120506 30-14120506 TiLink-C 14mm x 6mm x 5 deg Curved TiLink-C TYBER MEDICAL LLC