No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 00191375051480 | 305A-1009 | 305A-1009 | Tray Base 5" | PXN,LRP | Basic set-up tray,TRAY, SURGICAL | 1 | ENDOSKELETON® |
2 | M682230013150 | 2300-1315 | 2300-1315 | .25 SQ. Quick Connect Ratcheting T-Handle | OVD | Intervertebral fusion device with integrated fixation, lumbar | 2 | ENDOSKELETON® TAS |
3 | M682230013140 | 2300-1314 | 2300-1314 | Fixed Angle Driver Ancillary Handle | OVD,LXH | Intervertebral fusion device with integrated fixation, lumbar,Orthopedic Manual Intervertebral fusion device with integrated fixation, lumbar,Orthopedic Manual Surgical Instrument | 1 | ENDOSKELETON® TAS |
4 | M682230013130 | 2300-1313 | 2300-1313 | 40 Deg Fixed Angle Driver | LXH,OVD | Orthopedic Manual Surgical Instrument,Intervertebral fusion device with integrat Orthopedic Manual Surgical Instrument,Intervertebral fusion device with integrated fixation, lumbar | 1 | ENDOSKELETON® TAS |
5 | M682230013120 | 2300-1312 | 2300-1312 | Quick Inserter | OVD | Intervertebral fusion device with integrated fixation, lumbar | 2 | ENDOSKELETON® TAS |
6 | M682220000010 | 2200-0001 | 2200-0001 | IMPLANT CADDY | MQP | SPINAL VERTEBRAL BODY REPLACEMENT DEVICE | 2 | ENDOSKELETON TA VBR |
7 | M682215692200 | 2156-9220 | 2156-9220 | 7 DEG LORDOTIC, TRIAL, LARGE, 20MM | MQP | SPINAL VERTEBRAL BODY REPLACEMENT DEVICE | 2 | ENDOSKELETON TA VBR |
8 | M682215692180 | 2156-9218 | 2156-9218 | 7 DEG LORDOTIC, TRIAL, LARGE, 18MM | MQP | SPINAL VERTEBRAL BODY REPLACEMENT DEVICE | 2 | ENDOSKELETON TA VBR |
9 | M682215691200 | 2156-9120 | 2156-9120 | 7 DEG LORDOTIC, TRIAL, STANDARD, 20MM | MQP | SPINAL VERTEBRAL BODY REPLACEMENT DEVICE | 2 | ENDOSKELETON TA VBR |
10 | M682215691180 | 2156-9118 | 2156-9118 | 7 DEG LORDOTIC, TRIAL, STANDARD, 18MM | MQP | SPINAL VERTEBRAL BODY REPLACEMENT DEVICE | 2 | ENDOSKELETON TA VBR |
11 | M682215672200 | 2156-7220 | 2156-7220 | 7 DEG LORDOTIC, RASP, LARGE, 20MM | MQP | SPINAL VERTEBRAL BODY REPLACEMENT DEVICE | 2 | ENDOSKELETON TA VBR |
12 | M682215672180 | 2156-7218 | 2156-7218 | 7 DEG LORDOTIC, RASP, LARGE, 18MM | MQP | SPINAL VERTEBRAL BODY REPLACEMENT DEVICE | 2 | ENDOSKELETON TA VBR |
13 | M682215671200 | 2156-7120 | 2156-7120 | 7 DEG LORDOTIC, RASP, STANDARD, 20MM | MQP | SPINAL VERTEBRAL BODY REPLACEMENT DEVICE | 2 | ENDOSKELETON TA VBR |
14 | M682215671180 | 2156-7118 | 2156-7118 | 7 DEG LORDOTIC, RASP, STANDARD, 18MM | MQP | SPINAL VERTEBRAL BODY REPLACEMENT DEVICE | 2 | ENDOSKELETON TA VBR |
15 | 00191375052760 | 1379-030-001 | 1379-030-001 | Plate Instrument, Perforated Tray, Base | LRP | TRAY, SURGICAL | 1 | ENDOSKELETON® TAS |
16 | 00191375052548 | 1000-0068 | 1000-0068 | Anterolateral Impactor | OVD | Intervertebral fusion device with integrated fixation, lumbar | 2 | ENDOSKELETON® TAS |
17 | 00191375052081 | 905-020-001 | 905-020-001 | Double Bend Inserter Tray, Base | OVD | Intervertebral fusion device with integrated fixation, lumbar | 2 | ENDOSKELETON® TAS |
18 | 00191375051404 | 2900-1051 | 2900-1051 | 35mm Screw Caddy | OVD | Intervertebral fusion device with integrated fixation, lumbar | 2 | ENDOSKELETON® TAS |
19 | 00191375050445 | 2301-0006 | 2301-0006 | Plate Inserter, Oblique | OVD | Intervertebral fusion device with integrated fixation, lumbar | 2 | ENDOSKELETON® TAS |
20 | 00191375050438 | 2301-0005 | 2301-0005 | Plate Inserter, ALIF | OVD | Intervertebral fusion device with integrated fixation, lumbar | 2 | ENDOSKELETON® TAS |
21 | 00191375050421 | 2301-0007 | 2301-0007 | Lock Driver | OVD | Intervertebral fusion device with integrated fixation, lumbar | 2 | ENDOSKELETON® TAS |
22 | 00191375050414 | 2301-0004 | 2301-0004 | Awl Guide, Oblique | OVD | Intervertebral fusion device with integrated fixation, lumbar | 2 | ENDOSKELETON® TAS |
23 | 00191375050407 | 2301-0003 | 2301-0003 | Awl Guide, ALIF | OVD | Intervertebral fusion device with integrated fixation, lumbar | 2 | ENDOSKELETON® TAS |
24 | M682R14154100 | R14154-10 | R14154-10 | Wrench | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | ENDOSKELETON TL RETRACTOR |
25 | 00191375028338 | 2300-1317 | 2300-1317 | Graft Packing & Screw Reference Block | OVD | Intervertebral fusion device with integrated fixation, lumbar | 2 | ENDOSKELETON® TAS |
26 | 00191375028253 | 2900-1052 | 2900-1052 | Hyperlordotic Instrument Tray Sys, 16, 20° | OVD | Intervertebral fusion device with integrated fixation, lumbar | 2 | ENDOSKELETON® TAS |
27 | 00191375028246 | 2900-1050 | 2900-1050 | Hyperlordotic Instrument Tray System, 16, 20, 24° | OVD | Intervertebral fusion device with integrated fixation, lumbar | 2 | ENDOSKELETON® TAS |
28 | 00191375027737 | 2300-6535 | 2300-6535 | Interbody Fusion Device 6.5mm Implant Bone Screw 35mm | OVD | Intervertebral fusion device with integrated fixation, lumbar | 2 | ENDOSKELETON® TAS |
29 | 00191375025801 | 2300-1315 | 2300-1315 | .25 SQ. Quick Connect Ratcheting T-Handle | OVD | Intervertebral fusion device with integrated fixation, lumbar | 2 | ENDOSKELETON® TAS |
30 | 00191375025795 | 2300-1312 | 2300-1312 | Quick Inserter | OVD | Intervertebral fusion device with integrated fixation, lumbar | 2 | ENDOSKELETON® TAS |
31 | 00191375025733 | 2300-1314 | 2300-1314 | Fixed Angle Driver Ancillary Handle | LXH,OVD | Orthopedic Manual Surgical Instrument,Intervertebral fusion device with integrat Orthopedic Manual Surgical Instrument,Intervertebral fusion device with integrated fixation, lumbar | 1 | ENDOSKELETON® TAS |
32 | 00191375025726 | 2300-1313 | 2300-1313 | 40 Deg Fixed Angle Driver | OVD,LXH | Intervertebral fusion device with integrated fixation, lumbar,Orthopedic Manual Intervertebral fusion device with integrated fixation, lumbar,Orthopedic Manual Surgical Instrument | 1 | ENDOSKELETON® TAS |
33 | 00191375020608 | 3114-3116-S | 3114-3116-S | Interbody Fusion Device 4 Degree Oblique 16mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | ENDOSKELETON® TO Sterile Barrier System |
34 | 00191375020592 | 3114-3115-S | 3114-3115-S | Interbody Fusion Device 4 Degree Oblique 15mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | ENDOSKELETON® TO Sterile Barrier System |
35 | 00191375020585 | 3114-3114-S | 3114-3114-S | Interbody Fusion Device 4 Degree Oblique 14mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | ENDOSKELETON® TO Sterile Barrier System |
36 | 00191375020578 | 3114-3113-S | 3114-3113-S | Interbody Fusion Device 4 Degree Oblique 13mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | ENDOSKELETON® TO Sterile Barrier System |
37 | 00191375020561 | 3114-3112-S | 3114-3112-S | Interbody Fusion Device 4 Degree Oblique 12mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | ENDOSKELETON® TO Sterile Barrier System |
38 | 00191375020554 | 3114-3111-S | 3114-3111-S | Interbody Fusion Device 4 Degree Oblique 11mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | ENDOSKELETON® TO Sterile Barrier System |
39 | 00191375020547 | 3114-3110-S | 3114-3110-S | Interbody Fusion Device 4 Degree Oblique 10mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | ENDOSKELETON® TO Sterile Barrier System |
40 | 00191375020530 | 3114-3109-S | 3114-3109-S | Interbody Fusion Device 4 Degree Oblique 9mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | ENDOSKELETON® TO Sterile Barrier System |
41 | 00191375020523 | 3114-3108-S | 3114-3108-S | Interbody Fusion Device 4 Degree Oblique 8mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | ENDOSKELETON® TO Sterile Barrier System |
42 | 00191375020516 | 3114-2616-S | 3114-2616-S | Interbody Fusion Device 4 Degree PLIF 16mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | ENDOSKELETON® TO Sterile Barrier System |
43 | 00191375020509 | 3114-2615-S | 3114-2615-S | Interbody Fusion Device 4 Degree PLIF 15mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | ENDOSKELETON® TO Sterile Barrier System |
44 | 00191375020493 | 3114-2614-S | 3114-2614-S | Interbody Fusion Device 4 Degree PLIF 14mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | ENDOSKELETON® TO Sterile Barrier System |
45 | 00191375020486 | 3114-2613-S | 3114-2613-S | Interbody Fusion Device 4 Degree PLIF 13mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | ENDOSKELETON® TO Sterile Barrier System |
46 | 00191375020479 | 3114-2612-S | 3114-2612-S | Interbody Fusion Device 4 Degree PLIF 12mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | ENDOSKELETON® TO Sterile Barrier System |
47 | 00191375020462 | 3114-2611-S | 3114-2611-S | Interbody Fusion Device 4 Degree PLIF 11mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | ENDOSKELETON® TO Sterile Barrier System |
48 | 00191375020455 | 3114-2610-S | 3114-2610-S | Interbody Fusion Device 4 Degree PLIF 10mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | ENDOSKELETON® TO Sterile Barrier System |
49 | 00191375020448 | 3114-2609-S | 3114-2609-S | Interbody Fusion Device 4 Degree PLIF 9mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | ENDOSKELETON® TO Sterile Barrier System |
50 | 00191375020431 | 3114-2608-S | 3114-2608-S | Interbody Fusion Device 4 Degree PLIF 8mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | ENDOSKELETON® TO Sterile Barrier System |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 10852776006017 | PD-31-100 | PD-31-100 | The DTRAX Cervical Cage-T is a single-use, titanium alloy intervertebral implant The DTRAX Cervical Cage-T is a single-use, titanium alloy intervertebral implant available in various footprints and heights. It is intended to be used in cervical spinal fusion surgery for skeletally mature patients with degenerative disc disease of the cervical spine with accompanying radicular symptoms at one disc level. | DTRAX Cervical Cage-T | PROVIDENCE MEDICAL TECHNOLOGY, INC. |
2 | 10852776006000 | PD-31-200 | PD-31-200 | The DTRAX Cervical Cage-B is a single-use, titanium alloy intervertebral implant The DTRAX Cervical Cage-B is a single-use, titanium alloy intervertebral implant available in various footprints and heights. It is intended to be used in cervical spinal fusion surgery for skeletally mature patients with degenerative disc disease of the cervical spine with accompanying radicular symptoms at one disc level. | DTRAX Cervical Cage-B | PROVIDENCE MEDICAL TECHNOLOGY, INC. |
3 | 10840642162028 | SW18125-1410 | SW18125-1410 | Cervical Titanium Cage - Anatomical 17.5 mm x 14 mm x 10 mm | Stronghold® C 3D Titanium Interbody Device System | SPINE WAVE, INC. |
4 | 10840642162011 | SW18125-1409 | SW18125-1409 | Cervical Titanium Cage - Anatomical 17.5 mm x 14 mm x 9 mm | Stronghold® C 3D Titanium Interbody Device System | SPINE WAVE, INC. |
5 | 10840642162004 | SW18125-1408 | SW18125-1408 | Cervical Titanium Cage - Anatomical 17.5 mm x 14 mm x 8 mm | Stronghold® C 3D Titanium Interbody Device System | SPINE WAVE, INC. |
6 | 10840642161991 | SW18125-1407 | SW18125-1407 | Cervical Titanium Cage - Anatomical 17.5 mm x 14 mm x 7 mm | Stronghold® C 3D Titanium Interbody Device System | SPINE WAVE, INC. |
7 | 10840642161984 | SW18125-1406 | SW18125-1406 | Cervical Titanium Cage - Anatomical 17.5 mm x 14 mm x 6 mm | Stronghold® C 3D Titanium Interbody Device System | SPINE WAVE, INC. |
8 | 10840642161977 | SW18125-1405 | SW18125-1405 | Cervical Titanium Cage - Anatomical 17.5 mm x 14 mm x 5 mm | Stronghold® C 3D Titanium Interbody Device System | SPINE WAVE, INC. |
9 | 10840642161960 | SW18105-1015 | SW18105-1015 | Cervical Titanium Cage - Anatomical 15 mm x 12 mm x 10 mm | Stronghold® C 3D Titanium Interbody Device System | SPINE WAVE, INC. |
10 | 10840642161953 | SW18105-0915 | SW18105-0915 | Cervical Titanium Cage - Anatomical 15 mm x 12 mm x 9 mm | Stronghold® C 3D Titanium Interbody Device System | SPINE WAVE, INC. |
11 | 10840642161946 | SW18105-0815 | SW18105-0815 | Cervical Titanium Cage - Anatomical 15 mm x 12 mm x 8 mm | Stronghold® C 3D Titanium Interbody Device System | SPINE WAVE, INC. |
12 | 10840642161939 | SW18105-0715 | SW18105-0715 | Cervical Titanium Cage - Anatomical 15 mm x 12 mm x 7 mm | Stronghold® C 3D Titanium Interbody Device System | SPINE WAVE, INC. |
13 | 10840642161922 | SW18105-0615 | SW18105-0615 | Cervical Titanium Cage - Anatomical 15 mm x 12 mm x 6 mm | Stronghold® C 3D Titanium Interbody Device System | SPINE WAVE, INC. |
14 | 10840642161915 | SW18105-0515 | SW18105-0515 | Cervical Titanium Cage - Anatomical 15 mm x 12 mm x 5 mm | Stronghold® C 3D Titanium Interbody Device System | SPINE WAVE, INC. |
15 | 10840642161908 | SW18107-1412 | SW18107-1412 | Cervical Titanium Cage - Lordotic 17.5 mm x 14 mm x 12 mm | Stronghold® C 3D Titanium Interbody Device System | SPINE WAVE, INC. |
16 | 10840642161892 | SW18107-1411 | SW18107-1411 | Cervical Titanium Cage - Lordotic 17.5 mm x 14 mm x 11 mm | Stronghold® C 3D Titanium Interbody Device System | SPINE WAVE, INC. |
17 | 10840642161885 | SW18107-1410 | SW18107-1410 | Cervical Titanium Cage - Lordotic 17.5 mm x 14 mm x 10 mm | Stronghold® C 3D Titanium Interbody Device System | SPINE WAVE, INC. |
18 | 10840642161878 | SW18107-1409 | SW18107-1409 | Cervical Titanium Cage - Lordotic 17.5 mm x 14 mm x 9 mm | Stronghold® C 3D Titanium Interbody Device System | SPINE WAVE, INC. |
19 | 10840642161861 | SW18107-1408 | SW18107-1408 | Cervical Titanium Cage - Lordotic 17.5 mm x 14 mm x 8 mm | Stronghold® C 3D Titanium Interbody Device System | SPINE WAVE, INC. |
20 | 10840642161854 | SW18107-1407 | SW18107-1407 | Cervical Titanium Cage - Lordotic 17.5 mm x 14 mm x 7 mm | Stronghold® C 3D Titanium Interbody Device System | SPINE WAVE, INC. |
21 | 10840642161847 | SW18107-1406 | SW18107-1406 | Cervical Titanium Cage - Lordotic 17.5 mm x 14 mm x 6 mm | Stronghold® C 3D Titanium Interbody Device System | SPINE WAVE, INC. |
22 | 10840642161830 | SW18107-1405 | SW18107-1405 | Cervical Titanium Cage - Lordotic 17.5 mm x 14 mm x 5 mm | Stronghold® C 3D Titanium Interbody Device System | SPINE WAVE, INC. |
23 | 10840642161823 | SW18107-1215 | SW18107-1215 | Cervical Titanium Cage - Lordotic 15 mm x 12 mm x 12 mm | Stronghold® C 3D Titanium Interbody Device System | SPINE WAVE, INC. |
24 | 10840642161816 | SW18107-1115 | SW18107-1115 | Cervical Titanium Cage - Lordotic 15 mm x 12 mm x 11 mm | Stronghold® C 3D Titanium Interbody Device System | SPINE WAVE, INC. |
25 | 10840642161809 | SW18107-1015 | SW18107-1015 | Cervical Titanium Cage - Lordotic 15 mm x 12 mm x 10 mm | Stronghold® C 3D Titanium Interbody Device System | SPINE WAVE, INC. |
26 | 10840642161793 | SW18107-0915 | SW18107-0915 | Cervical Titanium Cage - Lordotic 15 mm x 12 mm x 9 mm | Stronghold® C 3D Titanium Interbody Device System | SPINE WAVE, INC. |
27 | 10840642161786 | SW18107-0815 | SW18107-0815 | Cervical Titanium Cage - Lordotic 15 mm x 12 mm x 8 mm | Stronghold® C 3D Titanium Interbody Device System | SPINE WAVE, INC. |
28 | 10840642161779 | SW18107-0715 | SW18107-0715 | Cervical Titanium Cage - Lordotic 15 mm x 12 mm x 7 mm | Stronghold® C 3D Titanium Interbody Device System | SPINE WAVE, INC. |
29 | 10840642161762 | SW18107-0615 | SW18107-0615 | Cervical Titanium Cage - Lordotic 15 mm x 12 mm x 6 mm | Stronghold® C 3D Titanium Interbody Device System | SPINE WAVE, INC. |
30 | 10840642161755 | SW18107-0515 | SW18107-0515 | Cervical Titanium Cage - Lordotic 15 mm x 12 mm x 5 mm | Stronghold® C 3D Titanium Interbody Device System | SPINE WAVE, INC. |
31 | 10840642149562 | 10-9060 | 10-9060 | Implant Inserter, Wide Depth Stop | Paramount® Anterior Cervical Spine System | SPINE WAVE, INC. |
32 | 10840642129649 | 10-5490 | 10-5490 | Implant Removal Tool, 14 mm x 12/13 mm | Paramount® Anterior Cervical Spine System | SPINE WAVE, INC. |
33 | 10840642129632 | 10-9019 | 10-9019 | Pull Rod, 15.5 mm x 14 mm | Paramount® Anterior Cervical Spine System | SPINE WAVE, INC. |
34 | 10840642129625 | 10-9056 | 10-9056 | Scoring Trial, T-handle | Paramount® Anterior Cervical Spine System | SPINE WAVE, INC. |
35 | 10840642129618 | 10-9049 | 10-9049 | Anatomic Scoring Trial, 8 mm x 15.5 mm x 14 mm (Modular) | Paramount® Anterior Cervical Spine System | SPINE WAVE, INC. |
36 | 10840642129601 | 10-9048 | 10-9048 | Anatomic Scoring Trial, 7 mm x 15.5 mm x 14 mm (Modular) | Paramount® Anterior Cervical Spine System | SPINE WAVE, INC. |
37 | 10840642129595 | 10-9047 | 10-9047 | Anatomic Scoring Trial, 6 mm x 15.5 mm x 14 mm (Modular) | Paramount® Anterior Cervical Spine System | SPINE WAVE, INC. |
38 | 10840642129588 | 10-9046 | 10-9046 | Anatomic Scoring Trial, 5 mm x 15.5 mm x 14 mm (Modular) | Paramount® Anterior Cervical Spine System | SPINE WAVE, INC. |
39 | 10840642129571 | 10-9045 | 10-9045 | Anatomic Scoring Trial, 8 mm x 14 mm x 12 mm (Modular) | Paramount® Anterior Cervical Spine System | SPINE WAVE, INC. |
40 | 10840642129564 | 10-9044 | 10-9044 | Anatomic Scoring Trial, 7 mm x 14 mm x 12 mm (Modular) | Paramount® Anterior Cervical Spine System | SPINE WAVE, INC. |
41 | 10840642129557 | 10-9043 | 10-9043 | Anatomic Scoring Trial, 6 mm x 14 mm x 12 mm (Modular) | Paramount® Anterior Cervical Spine System | SPINE WAVE, INC. |
42 | 10840642129540 | 10-9042 | 10-9042 | Anatomic Scoring Trial, 5 mm x 14 mm x 12 mm (Modular) | Paramount® Anterior Cervical Spine System | SPINE WAVE, INC. |
43 | 10840642129533 | 10-9041 | 10-9041 | Lordotic Scoring Trial, 10 mm x 15.5 mm x 14 mm (Modular) | Paramount® Anterior Cervical Spine System | SPINE WAVE, INC. |
44 | 10840642129526 | 10-9040 | 10-9040 | Lordotic Scoring Trial, 9 mm x 15.5 mm x 14 mm (Modular) | Paramount® Anterior Cervical Spine System | SPINE WAVE, INC. |
45 | 10840642129519 | 10-9039 | 10-9039 | Lordotic Scoring Trial, 8 mm x 15.5 mm x 14 mm (Modular) | Paramount® Anterior Cervical Spine System | SPINE WAVE, INC. |
46 | 10840642129502 | 10-9038 | 10-9038 | Lordotic Scoring Trial, 7 mm x 15.5 mm x 14 mm (Modular) | Paramount® Anterior Cervical Spine System | SPINE WAVE, INC. |
47 | 10840642129496 | 10-9037 | 10-9037 | Lordotic Scoring Trial, 6 mm x 15.5 mm x 14 mm (Modular) | Paramount® Anterior Cervical Spine System | SPINE WAVE, INC. |
48 | 10840642129489 | 10-9036 | 10-9036 | Lordotic Scoring Trial, 5 mm x 15.5 mm x 14 mm (Modular) | Paramount® Anterior Cervical Spine System | SPINE WAVE, INC. |
49 | 10840642129472 | 10-9035 | 10-9035 | Lordotic Scoring Trial, 10 mm x 14 mm x 12 mm (Modular) | Paramount® Anterior Cervical Spine System | SPINE WAVE, INC. |
50 | 10840642129465 | 10-9034 | 10-9034 | Lordotic Scoring Trial, 9 mm x 14 mm x 12 mm (Modular) | Paramount® Anterior Cervical Spine System | SPINE WAVE, INC. |