| No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
|---|---|---|---|---|---|---|---|---|
| 1 | 08057432561366 | PLS-5070T57 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 2 | 08057432561342 | SPS-27S550 | NDN,HXG | Cement, Bone, Vertebroplasty,Tamp | 1 | SPIDER KOLIBRI | ||
| 3 | 08057432561304 | PLS-555T540 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 4 | 08057432561144 | PLS-740T57 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 5 | 08057432561120 | PLS-730T57 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 6 | 08057432561090 | PLS-745T56 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 7 | 08057432560918 | PLS-540T540 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 8 | 08057432560895 | PLS-530T540 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 9 | 08057432560864 | LFC-002PK3209 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | TLIF LITE | ||
| 10 | 08057432560857 | LFC-002PK3207 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | TLIF LITE | ||
| 11 | 08057432560680 | PLS-1095T57 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 12 | 08057432560666 | SPS-26S645 | NDN,HXG | Cement, Bone, Vertebroplasty,Tamp | 1 | SPIDER KOLIBRI | ||
| 13 | 08057432560628 | SPS-26S540 | NDN,HXG | Cement, Bone, Vertebroplasty,Tamp | 1 | SPIDER KOLIBRI | ||
| 14 | 08057432564114 | PLS-840T55 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 15 | 08057432564077 | PLS-5095T540 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 16 | 08057432564060 | PLS-5090T540 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 17 | 08057432564053 | PLS-5085T540 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 18 | 08057432564039 | PLS-5075T540 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 19 | 08057432563995 | PLS-5095T56 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 20 | 08057432563964 | PLS-5080T56 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 21 | 08057432563933 | PLS-5065T56 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 22 | 08057432563926 | PLS-5100T55 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 23 | 08057432564497 | PLS-8080T57 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 24 | 08057432564480 | PLS-875T57 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 25 | 08057432564473 | PLS-870T57 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 26 | 08057432563889 | PLS-5080T55 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 27 | 08057432563858 | PLS-5065T55 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 28 | 08057432563810 | PLS-1085T58 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 29 | 08057432563803 | PLS-1080T58 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 30 | 08057432563797 | PLS-1075T58 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 31 | 08057432563711 | PLS-10080T58 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 32 | 08057432563698 | PLS-10070T58 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 33 | 08057432563629 | PLS-10035T58 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 34 | 08057432563612 | PLS-10030T58 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 35 | 08057432563599 | PLS-10095T57 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 36 | 08057432563520 | PLS-10060T57 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 37 | 08057432563513 | PLS-10055T57 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 38 | 08057432563490 | PLS-10045T57 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 39 | 08057432563360 | PLS-10055T56 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 40 | 08057432563353 | PLS-10050T56 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 41 | 08057432563308 | PLS-10100T55 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 42 | 08057432563285 | PLS-10090T55 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 43 | 08057432563247 | PLS-10070T55 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 44 | 08057432563223 | PLS-10060T55 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 45 | 08057432563216 | PLS-10055T55 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 46 | 08057432563179 | PLS-10035T55 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 47 | 08057432563131 | PLS-10090T540 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 48 | 08057432562967 | PLS-61T56 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 49 | 08057432562912 | PLS-960T58 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS | ||
| 50 | 08057432562899 | PLS-950T58 | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PLS |
| No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
|---|---|---|---|---|---|---|
| 1 | 00191375036005 | 2156-9319 | 2156-9319 | Trial, 7 Deg Lordotic, X-Large, 19mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
| 2 | 00191375036012 | 2156-9320 | 2156-9320 | Trial, 7 Deg Lordotic, X-Large, 20mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
| 3 | 00191375035992 | 2156-9318 | 2156-9318 | Trial, 7 Deg Lordotic, X-Large, 18mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
| 4 | 00191375035985 | 2156-9317 | 2156-9317 | Trial, 7 Deg Lordotic, X-Large, 17mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
| 5 | 00191375035978 | 2156-9219 | 2156-9219 | Trial, 7 Deg Lordotic, Large, 19mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
| 6 | 00191375035961 | 2156-9217 | 2156-9217 | Trial, 7 Deg Lordotic, Large, 17mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
| 7 | 00191375035954 | 2156-9119 | 2156-9119 | Trial, 7 Deg Lordotic, Standard, 19mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
| 8 | 00191375035947 | 2156-9117 | 2156-9117 | Trial, 7 Deg Lordotic, Standard, 17mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
| 9 | 00191375030287 | 2156-9316 | 2156-9316 | Trial, 7 Deg Lordotic, X-Large, 16mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
| 10 | 00191375030270 | 2156-9216 | 2156-9216 | Trial, 7 Deg Lordotic, Large, 16mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
| 11 | 00191375030263 | 2156-9116 | 2156-9116 | Trial, 7 Deg Lordotic, Standard, 16mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
| 12 | 00191375018896 | 2107-0320-S | 2107-0320-S | Interbody Fusion Device 7 Degree X-Large 20mm | ENDOSKELETON® TA VBR Sterile Barrier System | TITAN SPINE, LLC |
| 13 | 00191375018889 | 2107-0318-S | 2107-0318-S | Interbody Fusion Device 7 Degree X-Large 18mm | ENDOSKELETON® TA VBR Sterile Barrier System | TITAN SPINE, LLC |
| 14 | 00191375018872 | 2107-0220-S | 2107-0220-S | Interbody Fusion Device 7 Degree Large 20mm | ENDOSKELETON® TA VBR Sterile Barrier System | TITAN SPINE, LLC |
| 15 | 00191375018865 | 2107-0218-S | 2107-0218-S | Interbody Fusion Device 7 Degree Large 18mm | ENDOSKELETON® TA VBR Sterile Barrier System | TITAN SPINE, LLC |
| 16 | 00191375018858 | 2107-0120-S | 2107-0120-S | Interbody Fusion Device 7 Degree Standard 20mm | ENDOSKELETON® TA VBR Sterile Barrier System | TITAN SPINE, LLC |
| 17 | 00191375018841 | 2107-0118-S | 2107-0118-S | Interbody Fusion Device 7 Degree Standard 18mm | ENDOSKELETON® TA VBR Sterile Barrier System | TITAN SPINE, LLC |
| 18 | 00191375012030 | 2107-0320-N | 2107-0320-N | Interbody Fusion Device 7 Degree X-Large 20mm | ENDOSKELETON® TA VBR nanoLOCK® Surface Technology | TITAN SPINE, LLC |
| 19 | 00191375012023 | 2107-0318-N | 2107-0318-N | Interbody Fusion Device 7 Degree X-Large 18mm | ENDOSKELETON® TA VBR nanoLOCK® Surface Technology | TITAN SPINE, LLC |
| 20 | 00191375012016 | 2107-0220-N | Interbody Fusion Device 7 Degree Large 20mm | ENDOSKELETON® TA VBR nanoLOCK® Surface Technology | MEDTRONIC SOFAMOR DANEK, INC. | |
| 21 | 00191375012009 | 2107-0218-N | Interbody Fusion Device 7 Degree Large 18mm | ENDOSKELETON® TA VBR nanoLOCK® Surface Technology | MEDTRONIC SOFAMOR DANEK, INC. | |
| 22 | 00191375011996 | 2107-0120-N | Interbody Fusion Device 7 Degree Standard 20mm | ENDOSKELETON® TA VBR nanoLOCK® Surface Technology | MEDTRONIC SOFAMOR DANEK, INC. | |
| 23 | 00191375011989 | 2107-0118-N | Interbody Fusion Device 7 Degree Standard 18mm | ENDOSKELETON® TA VBR nanoLOCK® Surface Technology | MEDTRONIC SOFAMOR DANEK, INC. | |
| 24 | 00191375011972 | 1130-1010 | 1130-1010 | Caddy, Large | ENDOSKELETON® Sterile Barrier System | TITAN SPINE, LLC |
| 25 | 00191375011965 | 1130-1020 | 1130-1020 | Caddy, Medium | ENDOSKELETON® Sterile Barrier System | TITAN SPINE, LLC |
| 26 | 00191375011958 | 1130-1030 | 1130-1030 | Caddy, Small | ENDOSKELETON® Sterile Barrier System | TITAN SPINE, LLC |
| 27 | 00191375000143 | 2200-0001 | 2200-0001 | Implant Caddy | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
| 28 | 00191375000051 | 2107-0320 | 2107-0320 | Interbody Fusion Device 7 Degree X-Large 20mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
| 29 | 00191375000044 | 2107-0318 | 2107-0318 | Interbody Fusion Device 7 Degree X-Large 18mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
| 30 | 00191375000037 | 2107-0220 | Interbody Fusion Device 7 Degree Large 20mm | ENDOSKELETON® TA VBR | MEDTRONIC SOFAMOR DANEK, INC. | |
| 31 | 00191375000020 | 2107-0218 | Interbody Fusion Device 7 Degree Large 18mm | ENDOSKELETON® TA VBR | MEDTRONIC SOFAMOR DANEK, INC. | |
| 32 | 00191375000013 | 2107-0120 | Interbody Fusion Device 7 Degree Standard 20mm | ENDOSKELETON® TA VBR | MEDTRONIC SOFAMOR DANEK, INC. | |
| 33 | 00191375000006 | 2107-0118 | Interbody Fusion Device 7 Degree Standard 18mm | ENDOSKELETON® TA VBR | MEDTRONIC SOFAMOR DANEK, INC. | |
| 34 | 00191083043272 | 38-2670-9 | 38-2670-9 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
| 35 | 00191083043265 | 38-2670-7 | 38-2670-7 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
| 36 | 00191083042695 | 38-1435-11-6C | 38-1435-11-6C | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
| 37 | 00191083042688 | 38-2670-17 | 38-2670-17 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
| 38 | 00191083042671 | 38-2670-15 | 38-2670-15 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
| 39 | 00191083042664 | 38-2670-13 | 38-2670-13 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
| 40 | 00191083042657 | 38-2670-11 | 38-2670-11 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
| 41 | 00191083042640 | 38-2665-9 | 38-2665-9 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
| 42 | 00191083042633 | 38-2665-7 | 38-2665-7 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
| 43 | 00191083042626 | 38-2665-17 | 38-2665-17 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
| 44 | 00191083042619 | 38-2665-15 | 38-2665-15 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
| 45 | 00191083042602 | 38-2665-13 | 38-2665-13 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
| 46 | 00191083042077 | 38-2250-13 | 38-2250-13 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
| 47 | 00191083042596 | 38-2665-11 | 38-2665-11 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
| 48 | 00191083042589 | 38-2660-9 | 38-2660-9 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
| 49 | 00191083042572 | 38-2660-7 | 38-2660-7 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
| 50 | 00191083042565 | 38-2660-17 | 38-2660-17 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |