| No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
|---|---|---|---|---|---|---|---|---|
| 1 | 00887517399779 | 6942044 | CoRoent® XLR, 20x34x24 12° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 2 | 00887517399700 | 6941844 | CoRoent® XLR, 18x34x24 12° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 3 | 00887517399335 | 6941644 | CoRoent® XLR, 16x34x24 12° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 4 | 00887517398765 | 6941444 | CoRoent® XLR, 14x34x24 12° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 5 | 00887517398499 | 6941244 | CoRoent® XLR, 12x34x24 12° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 6 | 00887517398420 | 6941044 | CoRoent® XLR, 10x34x24 12° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 7 | 00887517398055 | 6932088 | CoRoent® XLR, 20x38x28 15° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 8 | 00887517397683 | 6931888 | CoRoent® XLR, 18x38x28 15° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 9 | 00887517397256 | 6931688 | CoRoent® XLR, 16x38x28 15° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 10 | 00887517396822 | 6931488 | CoRoent® XLR, 14x38x28 15° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 11 | 00887517396457 | 6931288 | CoRoent® XLR, 12x38x28 15° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 12 | 00887517395641 | 6922088 | CoRoent® XLR, 20x38x28 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 13 | 00887517395634 | 6922044 | CoRoent® XLR, 20x34x24 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 14 | 00887517395269 | 6921888 | CoRoent® XLR, 18x38x28 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 15 | 00887517395252 | 6921844 | CoRoent® XLR, 18x34x24 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 16 | 00887517394880 | 6921688 | CoRoent® XLR, 16x38x28 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 17 | 00887517394873 | 6921660 | CoRoent® XL Wide, 16x22x60mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 18 | 00887517394866 | 6921655 | CoRoent® XL Wide, 16x22x55mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 19 | 00887517394859 | 6921650 | CoRoent® XL Wide, 16x22x50mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 20 | 00887517394842 | 6921645 | CoRoent® XL Wide, 16x22x45mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 21 | 00887517394835 | 6921644 | CoRoent® XLR, 16x34x24 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 22 | 00887517394569 | 6921488 | CoRoent® XLR, 14x38x28 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 23 | 00887517394552 | 6921460 | CoRoent® XL Wide, 14x22x60mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 24 | 00887517394545 | 6921455 | CoRoent® XL Wide, 14x22x55mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 25 | 00887517394538 | 6921450 | CoRoent® XL Wide, 14x22x50mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 26 | 00887517394521 | 6921445 | CoRoent® XL Wide, 14x22x45mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 27 | 00887517394514 | 6921444 | CoRoent® XLR, 14x34x24 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 28 | 00887517394149 | 6921288 | CoRoent® XLR, 12x38x28 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 29 | 00887517394132 | 6921260 | CoRoent® XL Wide, 12x22x60mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 30 | 00887517394125 | 6921255 | CoRoent® XL Wide, 12x22x55mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 31 | 00887517394118 | 6921250 | CoRoent® XL Wide, 12x22x50mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 32 | 00887517394101 | 6921245 | CoRoent® XL Wide, 12x22x45mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 33 | 00887517393791 | 6921244 | CoRoent® XLR, 12x34x24 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 34 | 00887517393722 | 6921088 | CoRoent® XLR, 10x38x28 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 35 | 00887517393715 | 6921060 | CoRoent® XL Wide, 10x22x60mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 36 | 00887517393708 | 6921055 | CoRoent® XL Wide, 10x22x55mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 37 | 00887517393395 | 6921050 | CoRoent® XL Wide, 10x22x50mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 38 | 00887517393388 | 6921045 | CoRoent® XL Wide, 10x22x45mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 39 | 00887517393371 | 6921044 | CoRoent® XLR, 10x34x24 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 40 | 00887517393333 | 6920860 | CoRoent® XL Wide, 8x22x60mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 41 | 00887517393326 | 6920855 | CoRoent® XL Wide, 8x22x55mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 42 | 00887517393319 | 6920850 | CoRoent® XL Wide, 8x22x50mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 43 | 00887517393302 | 6920845 | CoRoent® XL Wide, 8x22x45mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 44 | 00887517392961 | 6916860 | CoRoent® XL, 16x18x60mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 45 | 00887517392954 | 6916855 | CoRoent® XL, 16x18x55mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 46 | 00887517392947 | 6916850 | CoRoent® XL, 16x18x50mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 47 | 00887517392930 | 6916845 | CoRoent® XL, 16x18x45mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 48 | 00887517392923 | 6916840 | CoRoent® XL, 16x18x40mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 49 | 00887517392916 | 6916260 | CoRoent® XL Wide, 16x22x60mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
| 50 | 00887517392909 | 6916255 | CoRoent® XL Wide, 16x22x55mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent |
| No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
|---|---|---|---|---|---|---|
| 1 | 00840180511619 | CI-11084-10-10227010 | LIF Trial, Rasped, 10 X 22 X 70, 10°, Hudson | General Instrument | ALPHATEC SPINE, INC. | |
| 2 | 00840180511619 | CI-11084-10-10227010 | LIF Trial, Rasped, 10 X 22 X 70, 10°, Hudson | General Instrument | ALPHATEC SPINE, INC. | |
| 3 | 00840180511602 | CI-11084-10-08227010 | LIF Trial, Rasped, 8 X 22 X 70, 10°, Hudson | General Instrument | ALPHATEC SPINE, INC. | |
| 4 | 00840180511602 | CI-11084-10-08227010 | LIF Trial, Rasped, 8 X 22 X 70, 10°, Hudson | General Instrument | ALPHATEC SPINE, INC. | |
| 5 | 00840180511596 | CI-11084-10-06227010 | LIF Trial, Rasped, 6 X 22 X 70, 10°, Hudson | General Instrument | ALPHATEC SPINE, INC. | |
| 6 | 00840180511596 | CI-11084-10-06227010 | LIF Trial, Rasped, 6 X 22 X 70, 10°, Hudson | General Instrument | ALPHATEC SPINE, INC. | |
| 7 | 00840180511589 | CI-11084-10-04227010 | LIF Trial, Rasped, 4 X 22 X 70, 10°, Hudson | General Instrument | ALPHATEC SPINE, INC. | |
| 8 | 00840180511589 | CI-11084-10-04227010 | LIF Trial, Rasped, 4 X 22 X 70, 10°, Hudson | General Instrument | ALPHATEC SPINE, INC. | |
| 9 | 00840180511572 | CI-11084-10-10187010 | LIF Trial, Rasped, 10 X 18 X 70, 10°, Hudson | General Instrument | ALPHATEC SPINE, INC. | |
| 10 | 00840180511572 | CI-11084-10-10187010 | LIF Trial, Rasped, 10 X 18 X 70, 10°, Hudson | General Instrument | ALPHATEC SPINE, INC. | |
| 11 | 00840180511565 | CI-11084-10-08187010 | LIF Trial, Rasped, 8 X 18 X 70, 10°, Hudson | General Instrument | ALPHATEC SPINE, INC. | |
| 12 | 00840180511565 | CI-11084-10-08187010 | LIF Trial, Rasped, 8 X 18 X 70, 10°, Hudson | General Instrument | ALPHATEC SPINE, INC. | |
| 13 | 00840180511558 | CI-11084-10-06187010 | LIF Trial, Rasped, 6 X 18 X 70, 10°, Hudson | General Instrument | ALPHATEC SPINE, INC. | |
| 14 | 00840180511558 | CI-11084-10-06187010 | LIF Trial, Rasped, 6 X 18 X 70, 10°, Hudson | General Instrument | ALPHATEC SPINE, INC. | |
| 15 | 00840180511541 | CI-11084-10-04187010 | LIF Trial, Rasped, 4 X 18 X 70, 10°, Hudson | General Instrument | ALPHATEC SPINE, INC. | |
| 16 | 00840180511541 | CI-11084-10-04187010 | LIF Trial, Rasped, 4 X 18 X 70, 10°, Hudson | General Instrument | ALPHATEC SPINE, INC. | |
| 17 | 00840180511251 | CI-11070-10-12227010 | LIF Trial, 1/3 Rasped, Grooves, 12 x 22 x 70 x 10° | General Instrument | ALPHATEC SPINE, INC. | |
| 18 | 00840180511251 | CI-11070-10-12227010 | LIF Trial, 1/3 Rasped, Grooves, 12 x 22 x 70 x 10° | General Instrument | ALPHATEC SPINE, INC. | |
| 19 | 00840180511244 | CI-11070-10-10227010 | LIF Trial, 1/3 Rasped, Grooves, 10 x 22 x 70 x 10° | General Instrument | ALPHATEC SPINE, INC. | |
| 20 | 00840180511244 | CI-11070-10-10227010 | LIF Trial, 1/3 Rasped, Grooves, 10 x 22 x 70 x 10° | General Instrument | ALPHATEC SPINE, INC. | |
| 21 | 00840180511237 | CI-11070-10-08227010 | LIF Trial, 1/3 Rasped, Grooves, 8 x 22 x 70 x 10° | General Instrument | ALPHATEC SPINE, INC. | |
| 22 | 00840180511237 | CI-11070-10-08227010 | LIF Trial, 1/3 Rasped, Grooves, 8 x 22 x 70 x 10° | General Instrument | ALPHATEC SPINE, INC. | |
| 23 | 00840180511220 | CI-11070-10-06227010 | LIF Trial, 1/3 Rasped, Grooves, 6 x 22 x 70 x 10° | General Instrument | ALPHATEC SPINE, INC. | |
| 24 | 00840180511220 | CI-11070-10-06227010 | LIF Trial, 1/3 Rasped, Grooves, 6 x 22 x 70 x 10° | General Instrument | ALPHATEC SPINE, INC. | |
| 25 | 00840180511213 | CI-11070-10-12187010 | LIF Trial, 1/3 Rasped, Grooves, 12 x 18 x 70 x 10° | General Instrument | ALPHATEC SPINE, INC. | |
| 26 | 00840180511213 | CI-11070-10-12187010 | LIF Trial, 1/3 Rasped, Grooves, 12 x 18 x 70 x 10° | General Instrument | ALPHATEC SPINE, INC. | |
| 27 | 00840180511206 | CI-11070-10-10187010 | LIF Trial, 1/3 Rasped, Grooves, 10 x 18 x 70 x 10° | General Instrument | ALPHATEC SPINE, INC. | |
| 28 | 00840180511206 | CI-11070-10-10187010 | LIF Trial, 1/3 Rasped, Grooves, 10 x 18 x 70 x 10° | General Instrument | ALPHATEC SPINE, INC. | |
| 29 | 00840180511190 | CI-11070-10-08187010 | LIF Trial, 1/3 Rasped, Grooves, 8 x 18 x 70 x 10° | General Instrument | ALPHATEC SPINE, INC. | |
| 30 | 00840180511190 | CI-11070-10-08187010 | LIF Trial, 1/3 Rasped, Grooves, 8 x 18 x 70 x 10° | General Instrument | ALPHATEC SPINE, INC. | |
| 31 | 00840180511183 | CI-11070-10-06187010 | LIF Trial, 1/3 Rasped, Grooves, 6 x 18 x 70 x 10° | General Instrument | ALPHATEC SPINE, INC. | |
| 32 | 00840180511183 | CI-11070-10-06187010 | LIF Trial, 1/3 Rasped, Grooves, 6 x 18 x 70 x 10° | General Instrument | ALPHATEC SPINE, INC. | |
| 33 | 00840180511176 | CI-11070-10-04187010 | LIF Trial, 1/3 Rasped, Grooves, 4 x 18 x 70 x 10° | General Instrument | ALPHATEC SPINE, INC. | |
| 34 | 00840180511176 | CI-11070-10-04187010 | LIF Trial, 1/3 Rasped, Grooves, 4 x 18 x 70 x 10° | General Instrument | ALPHATEC SPINE, INC. | |
| 35 | 00840180510711 | CI-11028 | Cranial Angled Trial Inserter, 15° | General Instrument | ALPHATEC SPINE, INC. | |
| 36 | 00840180510711 | CI-11028 | Cranial Angled Trial Inserter, 15° | General Instrument | ALPHATEC SPINE, INC. | |
| 37 | 00840180510490 | CI-11024 | Identiti ALIF SA, Squid, Modular Tip | General Instrument | ALPHATEC SPINE, INC. | |
| 38 | 00840180510490 | CI-11024 | Identiti ALIF SA, Squid, Modular Tip | General Instrument | ALPHATEC SPINE, INC. | |
| 39 | 00840180510438 | CI-10982 | Inserter/Distractor, Squid, Enlarged Slot | General Instrument | ALPHATEC SPINE, INC. | |
| 40 | 00840180510438 | CI-10982 | Inserter/Distractor, Squid, Enlarged Slot | General Instrument | ALPHATEC SPINE, INC. | |
| 41 | 00840180510339 | CI-11003-043828 | ALIF Trial Rasp Template, 4 x 38 x 28mm | General Instrument | ALPHATEC SPINE, INC. | |
| 42 | 00840180510339 | CI-11003-043828 | ALIF Trial Rasp Template, 4 x 38 x 28mm | General Instrument | ALPHATEC SPINE, INC. | |
| 43 | 00840180510322 | CI-11003-043424 | ALIF Trial Rasp Template, 4 x 34 x 24mm | General Instrument | ALPHATEC SPINE, INC. | |
| 44 | 00840180510322 | CI-11003-043424 | ALIF Trial Rasp Template, 4 x 34 x 24mm | General Instrument | ALPHATEC SPINE, INC. | |
| 45 | 00840180510087 | CI-10982-03 | Modular Inserter Distractor, IdentiTti ALIF Tip | General Instrument | ALPHATEC SPINE, INC. | |
| 46 | 00840180510087 | CI-10982-03 | Modular Inserter Distractor, IdentiTti ALIF Tip | General Instrument | ALPHATEC SPINE, INC. | |
| 47 | 00840180509999 | CI-10950 | Squid, Distractor Block, 34 x 24 x 10, 7° | General Instrument | ALPHATEC SPINE, INC. | |
| 48 | 00840180509999 | CI-10950 | Squid, Distractor Block, 34 x 24 x 10, 7° | General Instrument | ALPHATEC SPINE, INC. | |
| 49 | 00840180509807 | CI-11010-10-04141207 | Cervical Trial, 4 x 14 x 12, 7° | General Instrument | ALPHATEC SPINE, INC. | |
| 50 | 00840180509807 | CI-11010-10-04141207 | Cervical Trial, 4 x 14 x 12, 7° | General Instrument | ALPHATEC SPINE, INC. |