| No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
|---|---|---|---|---|---|---|---|---|
| 1 | 90814008025315 | PLE-015-S | PLIF Encoded 10x22 15mm 0 Degrees | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | nvp | |
| 2 | 90814008024974 | PLE-010-L | PLIF Encoded 10x30 10mm 0 Degree | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | nvp | |
| 3 | 90814008024967 | PLE-009-L | PLIF Encoded 10x30 9mm 0 Degree | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | nvp | |
| 4 | 90814008024950 | PLE-008-L | PLIF Encoded 10x30 8mm 0 Degree | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | nvp | |
| 5 | 90814008024943 | PLE-007-L | PLIF Encoded 10x30 7mm 0 Degree | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | nvp | |
| 6 | 90814008024936 | PLE-006-L | PLIF Encoded 10x30 6mm 0 Degree | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | nvp | |
| 7 | 90814008024929 | PLE-615-M | PLIF Encoded 10x26 15mm 6 Degree | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | nvp | |
| 8 | 90814008024912 | PLE-614-M | PLIF Encoded 10x26 14mm 6 Degree | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | nvp | |
| 9 | 90814008024905 | PLE-613-M | PLIF Encoded 10x26 13mm 6 Degree | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | nvp | |
| 10 | 90814008024899 | PLE-612-M | PLIF Encoded 10x26 12mm 6 Degree | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | nvp | |
| 11 | 90814008024882 | PLE-611-M | PLIF Encoded 10x26 11mm 6 Degree | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | nvp | |
| 12 | 90814008024875 | PLE-610-M | PLIF Encoded 10x26 10mm 6 Degree | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | nvp | |
| 13 | 90814008024868 | PLE-609-M | PLIF Encoded 10x26 9mm 6 Degree | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | nvp | |
| 14 | 90814008024851 | PLE-608-M | PLIF Encoded 10x26 8mm 6 Degree | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | nvp | |
| 15 | 90814008024844 | PLE-607-M | PLIF Encoded 10x26 7mm 6 Degree | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | nvp | |
| 16 | 90814008024837 | PLE-015-M | PLIF Encoded 10x26 15mm 0 Degrees | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | nvp | |
| 17 | 90814008024820 | PLE-014-M | PLIF Encoded 10x26 14mm 0 Degrees | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | nvp | |
| 18 | 90814008024813 | PLE-013-M | PLIF Encoded 10x26 13mm 0 Degrees | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | nvp | |
| 19 | 90814008024806 | PLE-012-M | PLIF Encoded 10x26 12mm 0 Degrees | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | nvp | |
| 20 | 90814008024790 | PLE-011-M | PLIF Encoded 10x26 11mm 0 Degrees | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | nvp | |
| 21 | 90814008024783 | PLE-010-M | PLIF Encoded 10x26 10mm 0 Degrees | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | nvp | |
| 22 | 90814008024776 | PLE-009-M | PLIF Encoded 10x26 9mm 0 Degrees | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | nvp | |
| 23 | 90814008024769 | PLE-008-M | PLIF Encoded 10x26 8mm 0 Degrees | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | nvp | |
| 24 | 90814008024752 | PLE-007-M | PLIF Encoded 10x26 7mm 0 Degrees | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | nvp | |
| 25 | 90814008024745 | PLE-006-M | PLIF Encoded 10x26 6mm 0 Degrees | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | nvp | |
| 26 | 90814008024738 | PLE-014-S | PLIF Encoded 10x22 14mm 0 Degrees | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | nvp | |
| 27 | 90814008024721 | PLE-013-S | PLIF Encoded 10x22 13mm 0 Degrees | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | nvp | |
| 28 | 90814008024714 | PLE-012-S | PLIF Encoded 10x22 12mm 0 Degrees | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | nvp | |
| 29 | 90814008024707 | PLE-011-S | PLIF Encoded 10x22 11mm 0 Degrees | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | nvp | |
| 30 | 90814008024691 | PLE-010-S | PLIF Encoded 10x22 10mm 0 Degrees | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | nvp | |
| 31 | 90814008024684 | PLE-009-S | PLIF Encoded 10x22 9mm 0 Degrees | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | nvp | |
| 32 | 90814008024677 | PLE-008-S | PLIF Encoded 10x22 8mm 0 Degrees | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | nvp | |
| 33 | 90814008024660 | PLE-007-S | PLIF Encoded 10x22 7mm 0 Degrees | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | nvp | |
| 34 | 90814008024653 | PLE-006-S | PLIF Encoded 10x22 6mm 0 Degrees | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | nvp | |
| 35 | 00810005664905 | PD-1000C-750 | Caddy 7.5 Screws. The FOCUS Pedicle Screw System is intended for use in the non Caddy 7.5 Screws. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. | LRP | Tray, Surgical | 1 | Focus | |
| 36 | 00810005664899 | PD-1000C-650 | Caddy 6.5 Screws. The FOCUS Pedicle Screw System is intended for use in the non Caddy 6.5 Screws. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. | LRP | Tray, Surgical | 1 | Focus | |
| 37 | 00810005662253 | PD-1000C-475 | Caddy 4.75 Screws. The FOCUS Pedicle Screw System is intended for use in the no Caddy 4.75 Screws. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. | LRP | Tray, Surgical | 1 | Focus | |
| 38 | 00810005662246 | PD-1000C-SS | Caddy Set Screws. The FOCUS Pedicle Screw System is intended for use in the non Caddy Set Screws. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. | LRP | Tray, Surgical | 1 | Focus | |
| 39 | 00810005662239 | PD-1000C-CC | Caddy CrossLinks. The FOCUS Pedicle Screw System is intended for use in the non Caddy CrossLinks. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. | LRP | Tray, Surgical | 1 | Focus | |
| 40 | 00810005662222 | PD-1000C-LR | Caddy Lordotic Rods. The FOCUS Pedicle Screw System is intended for use in the Caddy Lordotic Rods. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. | LRP | Tray, Surgical | 1 | Focus | |
| 41 | 00810005662215 | PD-1000C-SR | Caddy Straight Rods. The FOCUS Pedicle Screw System is intended for use in the Caddy Straight Rods. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. | LRP | Tray, Surgical | 1 | Focus | |
| 42 | 90814008024981 | PLE-011-L | PLIF Encoded 10x30 11mm 0 Degree | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | nvp | |
| 43 | 00810005662208 | PD-1000C-106 | Pedicle Screw Case 4 INSERT 4 Instruments. The FOCUS Pedicle Screw System is in Pedicle Screw Case 4 INSERT 4 Instruments. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. | LRP | Tray, Surgical | 1 | Focus | |
| 44 | 00810005662192 | PD-1000C-105 | Pedicle Screw Case 4 INSERT 3 Instruments. The FOCUS Pedicle Screw System is in Pedicle Screw Case 4 INSERT 3 Instruments. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. | LRP | Tray, Surgical | 1 | Focus | |
| 45 | 00810005662185 | PD-1000C-104 | Pedicle Screw Case 3 INSERT 2 Instruments. The FOCUS Pedicle Screw System is in Pedicle Screw Case 3 INSERT 2 Instruments. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. | LRP | Tray, Surgical | 1 | Focus | |
| 46 | 00810005662178 | PD-1000C-103 | Pedicle Screw Case 3 INSERT 1 Instruments. The FOCUS Pedicle Screw System is in Pedicle Screw Case 3 INSERT 1 Instruments. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. | LRP | Tray, Surgical | 1 | Focus | |
| 47 | 00810005662161 | PD-1000C-102 | Pedicle Screw Case, Instruments. The FOCUS Pedicle Screw System is intended for Pedicle Screw Case, Instruments. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. | LRP | Tray, Surgical | 1 | Focus | |
| 48 | 00810005662154 | PD-1000C-204 | Pedicle Screw Case 2 INSERT 3. The FOCUS Pedicle Screw System is intended for u Pedicle Screw Case 2 INSERT 3. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. | LRP | Tray, Surgical | 1 | Focus | |
| 49 | 00810005662147 | PD-1000C-211 | Pedicle Screw Case 2 Base, Implants. The FOCUS Pedicle Screw System is intended Pedicle Screw Case 2 Base, Implants. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. | LRP | Tray, Surgical | 1 | Focus | |
| 50 | 00810005662130 | PD-1000C-202 | Pedicle Screw Case 1 INSERT 2. The FOCUS Pedicle Screw System is intended for u Pedicle Screw Case 1 INSERT 2. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. | LRP | Tray, Surgical | 1 | Focus |
| No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
|---|---|---|---|---|---|---|
| 1 | 15060155711260 | 234-010-173 | 234-010-173 | The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbable Poly (l-lactic) Acid and Calcium Phosphate, which will be gradually resorbed into the body, this function however, is patient dependant. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 2 | 15060155711253 | 234-010-172 | 234-010-172 | The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbable Poly (l-lactic) Acid and Calcium Phosphate, which will be gradually resorbed into the body, this function however, is patient dependant. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 3 | 15060155711246 | 234-010-168 | 234-010-168 | The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbable Poly (L-latic) Acid and calcium phosphate which will be gradually resorbed into the body. This function however, is patient dependent. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 4 | 15060155711239 | 234-010-170 | 234-010-170 | The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbable Poly (L-latic) Acid and calcium phosphate which will be gradually resorbed into the body. This function however, is patient dependent. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 5 | 15060155711222 | 234-010-160 | 234-010-160 | The Biosteon® ACL Screw is a cannulated, single-use bone screw made of a resorba The Biosteon® ACL Screw is a cannulated, single-use bone screw made of a resorbable Poly (L-lactic) Acid and Calcium Phosphate which will be gradually resorbed into the body. this function however, is patient dependent. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 6 | 15060155711215 | 3910-200-086 | 3910-200-086 | The Biosteon® IntraLine® 6.5mm HA/PLLA Suture Anchor with three #2 Force Fibre®, The Biosteon® IntraLine® 6.5mm HA/PLLA Suture Anchor with three #2 Force Fibre®, is a single use device. It is made from a resorbable composite which will gradually be resorbed into the body. This function however is patient dependent. The device is supplied sterile. The device is intended to secure a suture or sutures to bone that are then used to reattach damaged soft tissue in orthopaedic procedures in the shoulder, foot/ankle, knee, hand/wrist, elbow and pelvis. The device is supplied with polyethylene sutures. | Biosteon® IntraLine® | BIOCOMPOSITES LTD |
| 7 | 15060155711208 | 3910-200-085 | 3910-200-085 | The Biosteon® IntraLine® 6.5mm HA/PLLA Needled Suture Anchor with two #2 Force F The Biosteon® IntraLine® 6.5mm HA/PLLA Needled Suture Anchor with two #2 Force Fibre®, is a single use device. It is made from a resorbable composite which will gradually be resorbed into the body. This function however is patient dependent. The device is supplied sterile. The device is intended to secure a suture or sutures to bone that are then used to reattach damaged soft tissue in orthopaedic procedures in the shoulder, foot/ankle, knee, hand/wrist, elbow and pelvis. The device is supplied with stainless steel needles and polyethylene sutures. | Biosteon® IntraLine® | BIOCOMPOSITES LTD |
| 8 | 15060155711192 | 3910-200-084 | 3910-200-084 | The Biosteon® IntraLine® 6.5mm HA/PLLA Suture Anchor with two #2 Force Fibre®, i The Biosteon® IntraLine® 6.5mm HA/PLLA Suture Anchor with two #2 Force Fibre®, is a single use device. It is made from a resorbable composite which will gradually be resorbed into the body. This function however is patient dependent. The device is supplied sterile. The device is intended to secure a suture or sutures to bone that are then used to reattach damaged soft tissue in orthopaedic procedures in the shoulder, foot/ankle, knee, hand/wrist, elbow and pelvis. The device is supplied with polyethylene sutures. | Biosteon® IntraLine® | BIOCOMPOSITES LTD |
| 9 | 15060155711185 | 3910-200-083 | 3910-200-083 | The Biosteon® IntraLine® 5.5mm HA/PLLA Suture Anchor with three #2 Force Fibre®, The Biosteon® IntraLine® 5.5mm HA/PLLA Suture Anchor with three #2 Force Fibre®, is a single use device. It is made from a resorbable composite which will gradually be resorbed into the body. This function however is patient dependent. The device is supplied sterile. The device is intended to secure a suture or sutures to bone that are then used to reattach damaged soft tissue in orthopaedic procedures in the shoulder, foot/ankle, knee, hand/wrist, elbow and pelvis. The device is supplied with polyethylene sutures. | Biosteon® IntraLine® | BIOCOMPOSITES LTD |
| 10 | 15060155711178 | 3910-200-082 | 3910-200-082 | The Biosteon® IntraLine® 5.5mm HA/PLLA Needled Suture Anchor with two #2 Force F The Biosteon® IntraLine® 5.5mm HA/PLLA Needled Suture Anchor with two #2 Force Fibre®, is a single use device. It is made from a resorbable composite which will gradually be resorbed into the body. This function however is patient dependent. The device is supplied sterile. The device is intended to secure a suture or sutures to bone that are then used to reattach damaged soft tissue in orthopaedic procedures in the shoulder, foot/ankle, knee, hand/wrist, elbow and pelvis. The device is supplied with stainless steel needles and polyethylene sutures. | Biosteon® IntraLine® | BIOCOMPOSITES LTD |
| 11 | 15060155711161 | 3910-200-081 | 3910-200-081 | The Biosteon® IntraLine® 5.5mm HA/PLLA Suture Anchor with two #2 Force Fibre®, i The Biosteon® IntraLine® 5.5mm HA/PLLA Suture Anchor with two #2 Force Fibre®, is a single use device. It is made from a resorbable composite which will gradually be resorbed into the body. This function however is patient dependent. The device is supplied sterile. The device is intended to secure a suture or sutures to bone that are then used to reattach damaged soft tissue in orthopaedic procedures in the shoulder, foot/ankle, knee, hand/wrist, elbow and pelvis. The device is supplied with polyethylene sutures. | Biosteon® IntraLine® | BIOCOMPOSITES LTD |
| 12 | 15060155711154 | 3910-200-080 | 3910-200-080 | The Biosteon® IntraLine 4.5mm HA/PLLA Suture Anchor with two #2 Force Fibre®, is The Biosteon® IntraLine 4.5mm HA/PLLA Suture Anchor with two #2 Force Fibre®, is a single use device. It is made from a resorbable composite which will gradually be resorbed into the body. This function however is patient dependent. The device is supplied sterile. The device is intended to secure a suture or sutures to bone that are then used to reattach damaged soft tissue in orthopaedic procedures in the shoulder, foot/ankle, knee, hand/wrist, elbow and pelvis. The device is supplied with polyethylene sutures. | Biosteon® IntraLine® | BIOCOMPOSITES LTD |
| 13 | 15060155710652 | 160-135T | 160-135T | The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok° Screw provides an interference fixation during femoral and/or tibial fixation in ACL reconstruction that resorbs and is replaced with bone during the healing process. Bilok® Screws are biodegradable and biocompatible. | Bilok® Screw | BIOCOMPOSITES LTD |
| 14 | 15060155710645 | 160-130T | 160-130T | The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok° Screw provides an interference fixation during femoral and/or tibial fixation in ACL reconstruction that resorbs and is replaced with bone during the healing process. Bilok® Screws are biodegradable and biocompatible. | Bilok® Screw | BIOCOMPOSITES LTD |
| 15 | 15060155710621 | 160-935T | 160-935T | The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok° Screw provides an interference fixation during femoral and/or tibial fixation in ACL reconstruction that resorbs and is replaced with bone during the healing process. Bilok® Screws are biodegradable and biocompatible. | Bilok® Screw | BIOCOMPOSITES LTD |
| 16 | 15060155710614 | 160-930T | 160-930T | The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok° Screw provides an interference fixation during femoral and/or tibial fixation in ACL reconstruction that resorbs and is replaced with bone during the healing process. Bilok® Screws are biodegradable and biocompatible. | Bilok® Screw | BIOCOMPOSITES LTD |
| 17 | 15060155710607 | 160-925T | 160-925T | The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok° Screw provides an interference fixation during femoral and/or tibial fixation in ACL reconstruction that resorbs and is replaced with bone during the healing process. Bilok® Screws are biodegradable and biocompatible. | Bilok® Screw | BIOCOMPOSITES LTD |
| 18 | 15060155710584 | 160-830T | 160-830T | The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok° Screw provides an interference fixation during femoral and/or tibial fixation in ACL reconstruction that resorbs and is replaced with bone during the healing process. Bilok® Screws are biodegradable and biocompatible. | Bilok® Screw | BIOCOMPOSITES LTD |
| 19 | 15060155710577 | 160-825T | 160-825T | The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok° Screw provides an interference fixation during femoral and/or tibial fixation in ACL reconstruction that resorbs and is replaced with bone during the healing process. Bilok® Screws are biodegradable and biocompatible. | Bilok® Screw | BIOCOMPOSITES LTD |
| 20 | 15060155710546 | 160-725T | 160-725T | The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok° Screw provides an interference fixation during femoral and/or tibial fixation in ACL reconstruction that resorbs and is replaced with bone during the healing process. Bilok® Screws are biodegradable and biocompatible and should not be used at an infected site. | Bilok® Screw | BIOCOMPOSITES LTD |
| 21 | 15060155710508 | 160-935ST | 160-935ST | The Bilok® ST Screw is a cannulated, sterile, single-use bone screw made of an a The Bilok® ST Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok® ST Screw is for use as a fixation screw in cruciate ligament surgery. It provides a combination of suspension and compression fixation that resorbs and it is subsequently replaced with bone during the healing process. Bilok® ST Screw is biodegradable and biocompatible. | Bilok® ST Screw | BIOCOMPOSITES LTD |
| 22 | 15060155710492 | 160-930ST | 160-930ST | The Bilok® ST Screw is a cannulated, sterile, single-use bone screw made of an a The Bilok® ST Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok® ST Screw is for use as a fixation screw in cruciate ligament surgery. It provides a combination of suspension and compression fixation that resorbs and it is subsequently replaced with bone during the healing process. Bilok® ST Screw is biodegradable and biocompatible. | Bilok® ST Screw | BIOCOMPOSITES LTD |
| 23 | 15060155710362 | 234-500-350 | 234-500-350 | The Biosteon® Cross Pin is a bioabsorbable HA/PLLA, for surgical reconstruction The Biosteon® Cross Pin is a bioabsorbable HA/PLLA, for surgical reconstruction of anterior cruciate ligament (ACL) deficient knee to provide cross pin femoral fixation of the various soft tissue ACL autografts and allografts. | Biosteon® Cross Pin | BIOCOMPOSITES LTD |
| 24 | 15060155710355 | 234-500-340 | 234-500-340 | The Biosteon® Cross Pin is a bioabsorbable HA/PLLA, for surgical reconstruction The Biosteon® Cross Pin is a bioabsorbable HA/PLLA, for surgical reconstruction of anterior cruciate ligament (ACL) deficient knee to provide cross pin femoral fixation of the various soft tissue ACL autografts and allografts. | Biosteon® Cross Pin | BIOCOMPOSITES LTD |
| 25 | 15060155710348 | 234-010-180 | 234-010-180 | The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbable Poly (l-lactic) Acid and Calcium Phosphate, which will be gradually resorbed into the body, this function however, is patient dependant. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 26 | 15060155710331 | 234-010-179 | 234-010-179 | The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbable Poly (l-lactic) Acid and Calcium Phosphate, which will be gradually resorbed into the body, this function however, is patient dependant. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 27 | 15060155710324 | 234-010-178 | 234-010-178 | The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbable Poly (l-lactic) Acid and Calcium Phosphate, which will be gradually resorbed into the body, this function however, is patient dependant. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 28 | 15060155710317 | 234-010-177 | 234-010-177 | The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbable Poly (l-lactic) Acid and Calcium Phosphate, which will be gradually resorbed into the body, this function however, is patient dependant. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 29 | 15060155710300 | 234-010-167 | 234-010-167 | The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbable Poly (l-lactic) Acid and Calcium Phosphate, which will be gradually resorbed into the body, this function however, is patient dependant. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 30 | 15060155710294 | 234-010-166 | 234-010-166 | The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbable Poly (l-lactic) Acid and Calcium Phosphate, which will be gradually resorbed into the body, this function however, is patient dependant. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 31 | 15060155710287 | 234-010-165 | 234-010-165 | The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbable Poly (l-lactic) Acid and Calcium Phosphate, which will be gradually resorbed into the body, this function however, is patient dependant. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 32 | 15060155710270 | 234-010-164 | 234-010-164 | The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbable Poly (L-latic) Acid and calcium phosphate which will be gradually resorbed into the body. This function however, is patient dependent. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 33 | 15060155710263 | 234-010-163 | 234-010-163 | The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbable Poly (L-latic) Acid and calcium phosphate which will be gradually resorbed into the body. This function however, is patient dependent. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 34 | 15060155710256 | 234-010-162 | 234-010-162 | The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbable Poly (L-latic) Acid and calcium phosphate which will be gradually resorbed into the body. This function however, is patient dependent. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 35 | 15060155710249 | 234-010-161 | 234-010-161 | The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbable Poly (L-latic) Acid and calcium phosphate which will be gradually resorbed into the body. This function however, is patient dependent. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 36 | 14061144348987 | GP001A.076.031.MH | GP001A.076.031 STE | GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
| 37 | 14053613285541 | OC06D.076.032 | OC06D.076.032.STE | GUIDE PIN & GUIDE SCREW SET | GEBR. BRASSELER GMBH & CO. KG | |
| 38 | 14053613285534 | OC907P.067.032 | OC907P.067.032 STE | GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
| 39 | 14053613285329 | GS905.050.032.M5 | GS905.050.032.STE | KOMET GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
| 40 | 14053613285145 | 02-029-99-1004 | 02-029-99-1004 | GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
| 41 | 14053613284780 | GP007.075.032.K4 | GP007.075.032 | KOMET GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
| 42 | 14053613284766 | GS901.033.032.K4 | GS901.033.032 | KOMET GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
| 43 | 14053613284391 | OC06Z.127.032 | OC06Z.127.032 STE | GUIDE PIN SET | GEBR. BRASSELER GMBH & CO. KG | |
| 44 | 14053613284384 | OC04N.127.032 | OC04N.127.032 STE | GUIDE PIN SET | GEBR. BRASSELER GMBH & CO. KG | |
| 45 | 14053613284377 | OC06D.067.032 | OC06D.067.032 STE | GUIDE PIN & GUIDE SCREW SET | GEBR. BRASSELER GMBH & CO. KG | |
| 46 | 14053613284223 | GP007A.076.031 | GP007A.076.031 STE | GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
| 47 | 14053613283837 | OC005.067.032 STE | OC005.067.032 STE | GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
| 48 | 14053613282625 | GP003A.027.030.M5 | GP003A.027.030 STE | KOMET GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
| 49 | 14053613282601 | OC002A.089.032 STE | OC002A.089.032 STE | GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
| 50 | 14053613282069 | GP005.067.032.M5 | GP005.067.032 STE | KOMET GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG |