| No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
|---|---|---|---|---|---|---|---|---|
| 1 | 00841732101869 | 100.7097 | Rod Template, D5.5xL400mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | GENERIC INSTRUMENTS | |
| 2 | 00841732109001 | 016.7072 | Cutter, Sleeve, Type 2 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | PICASSO MIS Spinal System | |
| 3 | 00841732108998 | 016.7064 | Anti-Torque Device | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | PICASSO MIS Spinal System | |
| 4 | 00841732108981 | 016.7063 | Hex Driver with Torque Limiting T-Handle, 4.5 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | PICASSO MIS Spinal System | |
| 5 | 00841732108974 | 016.7062 | Hex Driver, Shaft, 1/4" Square Male QC, 4.5 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | PICASSO MIS Spinal System | |
| 6 | 00841732108967 | 016.7061 | Hex Driver with Handle, Self-Retention, 4.5 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | PICASSO MIS Spinal System | |
| 7 | 00841732108950 | 016.7052 | Hex Driver with Handle, 3.0 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | PICASSO MIS Spinal System | |
| 8 | 00841732108943 | 016.7051 | Rod Inserter | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | PICASSO MIS Spinal System | |
| 9 | 00841732108936 | 016.7042 | Alignment Tool, Percutaneous Screw Head | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | PICASSO MIS Spinal System | |
| 10 | 00841732108929 | 016.7100 | Hex Driver, Cannulated, 1/4" Square QC, 4.0 Self-Retention | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | PICASSO MIS Spinal System | |
| 11 | 00841732108912 | 016.7041 | Hex Driver, Cannulated, 1/4" Square Male QC, 4.0 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | PICASSO MIS Spinal System | |
| 12 | 00841732108905 | 016.7034 | Tap, Cannulated, 1/4" Square Male QC, 6.5 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | PICASSO MIS Spinal System | |
| 13 | 00841732108899 | 016.7033 | Tap, Cannulated, 1/4" Square Male QC, 5.5 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | PICASSO MIS Spinal System | |
| 14 | 00841732108882 | 016.7032 | Tap, Cannulated, 1/4" Square Male QC, 4.5 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | PICASSO MIS Spinal System | |
| 15 | 00841732108875 | 016.7021 | Drill, Trilobe End, D3.4 (for 4.5/5.0/5.5 Screws) | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | PICASSO MIS Spinal System | |
| 16 | 00841732108868 | 016.7014 | Dilator, ID14 x OD17mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | PICASSO MIS Spinal System | |
| 17 | 00841732108851 | 016.7012 | Dilator, ID10 x OD14mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | PICASSO MIS Spinal System | |
| 18 | 00841732108844 | 016.7011 | Dilator, ID1.8 x OD10mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | PICASSO MIS Spinal System | |
| 19 | 00841732108837 | 016.6200 | Percutaneous Straight Rod, D6.0 x L200mm | MNI | ORTHOSIS, SPINAL PEDICLE FIXATION | 2 | PICASSO MIS Spinal System | |
| 20 | 00841732108820 | 016.6160 | Percutaneous Straight Rod, D6.0 x L160mm | MNI | ORTHOSIS, SPINAL PEDICLE FIXATION | 2 | PICASSO MIS Spinal System | |
| 21 | 00841732108813 | 016.6150 | Percutaneous Straight Rod, D6.0 x L150mm | MNI | ORTHOSIS, SPINAL PEDICLE FIXATION | 2 | PICASSO MIS Spinal System | |
| 22 | 00841732108806 | 016.6140 | Percutaneous Straight Rod, D6.0 x L140mm | MNI | ORTHOSIS, SPINAL PEDICLE FIXATION | 2 | PICASSO MIS Spinal System | |
| 23 | 00841732108790 | 016.6130 | Percutaneous Straight Rod, D6.0 x L130mm | MNI | ORTHOSIS, SPINAL PEDICLE FIXATION | 2 | PICASSO MIS Spinal System | |
| 24 | 00841732108783 | 016.6120 | Percutaneous Straight Rod, D6.0 x L120mm | MNI | ORTHOSIS, SPINAL PEDICLE FIXATION | 2 | PICASSO MIS Spinal System | |
| 25 | 00841732108776 | 016.6110 | Percutaneous Straight Rod, D6.0 x L110mm | MNI | ORTHOSIS, SPINAL PEDICLE FIXATION | 2 | PICASSO MIS Spinal System | |
| 26 | 00841732108769 | 016.6100 | Percutaneous Straight Rod, D6.0 x L100mm | MNI | ORTHOSIS, SPINAL PEDICLE FIXATION | 2 | PICASSO MIS Spinal System | |
| 27 | 00841732108752 | 016.6090 | Percutaneous Straight Rod, D6.0 x L90mm | MNI | ORTHOSIS, SPINAL PEDICLE FIXATION | 2 | PICASSO MIS Spinal System | |
| 28 | 00841732108745 | 016.6080 | Percutaneous Straight Rod, D6.0 x L80mm | MNI | ORTHOSIS, SPINAL PEDICLE FIXATION | 2 | PICASSO MIS Spinal System | |
| 29 | 00841732108738 | 016.6070 | Percutaneous Straight Rod, D6.0 x L70mm | MNI | ORTHOSIS, SPINAL PEDICLE FIXATION | 2 | PICASSO MIS Spinal System | |
| 30 | 00841732108721 | 016.6065 | Percutaneous Straight Rod, D6.0 x L65mm | MNI | ORTHOSIS, SPINAL PEDICLE FIXATION | 2 | PICASSO MIS Spinal System | |
| 31 | 00841732108714 | 016.6060 | Percutaneous Straight Rod, D6.0 x L60mm | MNI | ORTHOSIS, SPINAL PEDICLE FIXATION | 2 | PICASSO MIS Spinal System | |
| 32 | 00841732108707 | 016.6055 | Percutaneous Straight Rod, D6.0 x L55mm | MNI | ORTHOSIS, SPINAL PEDICLE FIXATION | 2 | PICASSO MIS Spinal System | |
| 33 | 00841732108691 | 016.6050 | Percutaneous Straight Rod, D6.0 x L50mm | MNI | ORTHOSIS, SPINAL PEDICLE FIXATION | 2 | PICASSO MIS Spinal System | |
| 34 | 00841732108684 | 016.6045 | Percutaneous Straight Rod, D6.0 x L45mm | MNI | ORTHOSIS, SPINAL PEDICLE FIXATION | 2 | PICASSO MIS Spinal System | |
| 35 | 00841732108677 | 016.6040 | Percutaneous Straight Rod, D6.0 x L40mm | MNI | ORTHOSIS, SPINAL PEDICLE FIXATION | 2 | PICASSO MIS Spinal System | |
| 36 | 00841732108660 | 016.6035 | Percutaneous Straight Rod, D6.0 x L35mm | MNI | ORTHOSIS, SPINAL PEDICLE FIXATION | 2 | PICASSO MIS Spinal System | |
| 37 | 00841732108653 | 016.3150 | Percutaneous Curved Rod, D6.0 x L150mm | MNI | ORTHOSIS, SPINAL PEDICLE FIXATION | 2 | PICASSO MIS Spinal System | |
| 38 | 00841732108646 | 016.3140 | Percutaneous Curved Rod, D6.0 x L140mm | MNI | ORTHOSIS, SPINAL PEDICLE FIXATION | 2 | PICASSO MIS Spinal System | |
| 39 | 00841732108639 | 016.3130 | Percutaneous Curved Rod, D6.0 x L130mm | MNI | ORTHOSIS, SPINAL PEDICLE FIXATION | 2 | PICASSO MIS Spinal System | |
| 40 | 00841732108622 | 016.3120 | Percutaneous Curved Rod, D6.0 x L120mm | MNI | ORTHOSIS, SPINAL PEDICLE FIXATION | 2 | PICASSO MIS Spinal System | |
| 41 | 00841732108615 | 016.3110 | Percutaneous Curved Rod, D6.0 x L110mm | MNI | ORTHOSIS, SPINAL PEDICLE FIXATION | 2 | PICASSO MIS Spinal System | |
| 42 | 00841732108608 | 016.3100 | Percutaneous Curved Rod, D6.0 x L100mm | MNI | ORTHOSIS, SPINAL PEDICLE FIXATION | 2 | PICASSO MIS Spinal System | |
| 43 | 00841732108592 | 016.3095 | Percutaneous Curved Rod, D6.0 x L95mm | MNI | ORTHOSIS, SPINAL PEDICLE FIXATION | 2 | PICASSO MIS Spinal System | |
| 44 | 00841732108585 | 016.3090 | Percutaneous Curved Rod, D6.0 x L90mm | MNI | ORTHOSIS, SPINAL PEDICLE FIXATION | 2 | PICASSO MIS Spinal System | |
| 45 | 00841732108578 | 016.3085 | Percutaneous Curved Rod, D6.0 x L85mm | MNI | ORTHOSIS, SPINAL PEDICLE FIXATION | 2 | PICASSO MIS Spinal System | |
| 46 | 00841732108561 | 016.3080 | Percutaneous Curved Rod, D6.0 x L80mm | MNI | ORTHOSIS, SPINAL PEDICLE FIXATION | 2 | PICASSO MIS Spinal System | |
| 47 | 00841732108554 | 016.3075 | Percutaneous Curved Rod, D6.0 x L75mm | MNI | ORTHOSIS, SPINAL PEDICLE FIXATION | 2 | PICASSO MIS Spinal System | |
| 48 | 00841732108547 | 016.3070 | Percutaneous Curved Rod, D6.0 x L70mm | MNI | ORTHOSIS, SPINAL PEDICLE FIXATION | 2 | PICASSO MIS Spinal System | |
| 49 | 00841732108530 | 016.3065 | Percutaneous Curved Rod, D6.0 x L65mm | MNI | ORTHOSIS, SPINAL PEDICLE FIXATION | 2 | PICASSO MIS Spinal System | |
| 50 | 00841732108523 | 016.3060 | Percutaneous Curved Rod, D6.0 x L60mm | MNI | ORTHOSIS, SPINAL PEDICLE FIXATION | 2 | PICASSO MIS Spinal System |
| No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
|---|---|---|---|---|---|---|
| 1 | 00370049613881 | 100114842 | 100114842 | The SUPSTANCE Small VBR system is a PEEK Optima vertebral body replacement (VBR) The SUPSTANCE Small VBR system is a PEEK Optima vertebral body replacement (VBR) system intended to replace a vertebral body. It is designed for use in the cervical and in the thoracolumbar spine (C3 - L5) to replace a collapsed, damaged or unstable vertebral body during tumor or trauma management and to replace a partially removed vertebral body in the management of degenerative disorders. | SUPSTANCE Small | H.P.I. |
| 2 | 00191375036005 | 2156-9319 | 2156-9319 | Trial, 7 Deg Lordotic, X-Large, 19mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
| 3 | 00191375036012 | 2156-9320 | 2156-9320 | Trial, 7 Deg Lordotic, X-Large, 20mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
| 4 | 00191375035992 | 2156-9318 | 2156-9318 | Trial, 7 Deg Lordotic, X-Large, 18mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
| 5 | 00191375035985 | 2156-9317 | 2156-9317 | Trial, 7 Deg Lordotic, X-Large, 17mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
| 6 | 00191375035978 | 2156-9219 | 2156-9219 | Trial, 7 Deg Lordotic, Large, 19mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
| 7 | 00191375035961 | 2156-9217 | 2156-9217 | Trial, 7 Deg Lordotic, Large, 17mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
| 8 | 00191375035954 | 2156-9119 | 2156-9119 | Trial, 7 Deg Lordotic, Standard, 19mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
| 9 | 00191375035947 | 2156-9117 | 2156-9117 | Trial, 7 Deg Lordotic, Standard, 17mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
| 10 | 00191375030287 | 2156-9316 | 2156-9316 | Trial, 7 Deg Lordotic, X-Large, 16mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
| 11 | 00191375030270 | 2156-9216 | 2156-9216 | Trial, 7 Deg Lordotic, Large, 16mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
| 12 | 00191375030263 | 2156-9116 | 2156-9116 | Trial, 7 Deg Lordotic, Standard, 16mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
| 13 | 00191375018896 | 2107-0320-S | 2107-0320-S | Interbody Fusion Device 7 Degree X-Large 20mm | ENDOSKELETON® TA VBR Sterile Barrier System | TITAN SPINE, LLC |
| 14 | 00191375018889 | 2107-0318-S | 2107-0318-S | Interbody Fusion Device 7 Degree X-Large 18mm | ENDOSKELETON® TA VBR Sterile Barrier System | TITAN SPINE, LLC |
| 15 | 00191375018872 | 2107-0220-S | 2107-0220-S | Interbody Fusion Device 7 Degree Large 20mm | ENDOSKELETON® TA VBR Sterile Barrier System | TITAN SPINE, LLC |
| 16 | 00191375018865 | 2107-0218-S | 2107-0218-S | Interbody Fusion Device 7 Degree Large 18mm | ENDOSKELETON® TA VBR Sterile Barrier System | TITAN SPINE, LLC |
| 17 | 00191375018858 | 2107-0120-S | 2107-0120-S | Interbody Fusion Device 7 Degree Standard 20mm | ENDOSKELETON® TA VBR Sterile Barrier System | TITAN SPINE, LLC |
| 18 | 00191375018841 | 2107-0118-S | 2107-0118-S | Interbody Fusion Device 7 Degree Standard 18mm | ENDOSKELETON® TA VBR Sterile Barrier System | TITAN SPINE, LLC |
| 19 | 00191375012030 | 2107-0320-N | 2107-0320-N | Interbody Fusion Device 7 Degree X-Large 20mm | ENDOSKELETON® TA VBR nanoLOCK® Surface Technology | TITAN SPINE, LLC |
| 20 | 00191375012023 | 2107-0318-N | 2107-0318-N | Interbody Fusion Device 7 Degree X-Large 18mm | ENDOSKELETON® TA VBR nanoLOCK® Surface Technology | TITAN SPINE, LLC |
| 21 | 00191375012016 | 2107-0220-N | Interbody Fusion Device 7 Degree Large 20mm | ENDOSKELETON® TA VBR nanoLOCK® Surface Technology | MEDTRONIC SOFAMOR DANEK, INC. | |
| 22 | 00191375012009 | 2107-0218-N | Interbody Fusion Device 7 Degree Large 18mm | ENDOSKELETON® TA VBR nanoLOCK® Surface Technology | MEDTRONIC SOFAMOR DANEK, INC. | |
| 23 | 00191375011996 | 2107-0120-N | Interbody Fusion Device 7 Degree Standard 20mm | ENDOSKELETON® TA VBR nanoLOCK® Surface Technology | MEDTRONIC SOFAMOR DANEK, INC. | |
| 24 | 00191375011989 | 2107-0118-N | Interbody Fusion Device 7 Degree Standard 18mm | ENDOSKELETON® TA VBR nanoLOCK® Surface Technology | MEDTRONIC SOFAMOR DANEK, INC. | |
| 25 | 00191375011972 | 1130-1010 | 1130-1010 | Caddy, Large | ENDOSKELETON® Sterile Barrier System | TITAN SPINE, LLC |
| 26 | 00191375011965 | 1130-1020 | 1130-1020 | Caddy, Medium | ENDOSKELETON® Sterile Barrier System | TITAN SPINE, LLC |
| 27 | 00191375011958 | 1130-1030 | 1130-1030 | Caddy, Small | ENDOSKELETON® Sterile Barrier System | TITAN SPINE, LLC |
| 28 | 00191375000143 | 2200-0001 | 2200-0001 | Implant Caddy | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
| 29 | 00191375000051 | 2107-0320 | 2107-0320 | Interbody Fusion Device 7 Degree X-Large 20mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
| 30 | 00191375000044 | 2107-0318 | 2107-0318 | Interbody Fusion Device 7 Degree X-Large 18mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
| 31 | 00191375000037 | 2107-0220 | Interbody Fusion Device 7 Degree Large 20mm | ENDOSKELETON® TA VBR | MEDTRONIC SOFAMOR DANEK, INC. | |
| 32 | 00191375000020 | 2107-0218 | Interbody Fusion Device 7 Degree Large 18mm | ENDOSKELETON® TA VBR | MEDTRONIC SOFAMOR DANEK, INC. | |
| 33 | 00191375000013 | 2107-0120 | Interbody Fusion Device 7 Degree Standard 20mm | ENDOSKELETON® TA VBR | MEDTRONIC SOFAMOR DANEK, INC. | |
| 34 | 00191375000006 | 2107-0118 | Interbody Fusion Device 7 Degree Standard 18mm | ENDOSKELETON® TA VBR | MEDTRONIC SOFAMOR DANEK, INC. | |
| 35 | 00191083043272 | 38-2670-9 | 38-2670-9 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
| 36 | 00191083043265 | 38-2670-7 | 38-2670-7 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
| 37 | 00191083042695 | 38-1435-11-6C | 38-1435-11-6C | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
| 38 | 00191083042688 | 38-2670-17 | 38-2670-17 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
| 39 | 00191083042671 | 38-2670-15 | 38-2670-15 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
| 40 | 00191083042664 | 38-2670-13 | 38-2670-13 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
| 41 | 00191083042657 | 38-2670-11 | 38-2670-11 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
| 42 | 00191083042640 | 38-2665-9 | 38-2665-9 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
| 43 | 00191083042633 | 38-2665-7 | 38-2665-7 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
| 44 | 00191083042626 | 38-2665-17 | 38-2665-17 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
| 45 | 00191083042619 | 38-2665-15 | 38-2665-15 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
| 46 | 00191083042602 | 38-2665-13 | 38-2665-13 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
| 47 | 00191083042077 | 38-2250-13 | 38-2250-13 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
| 48 | 00191083042596 | 38-2665-11 | 38-2665-11 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
| 49 | 00191083042589 | 38-2660-9 | 38-2660-9 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
| 50 | 00191083042572 | 38-2660-7 | 38-2660-7 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |