No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | M711CRT006ST0 | CRT006ST | CP Ti | GWO | Plate, Cranioplasty, Preformed, Alterable | 2 | Neuro & Craniofacial Fixation System | |
2 | M711E20024 | E2002 | E2002 | KWQ,KWP,MNH,MNI,NKB | Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Inte Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease | Excella II® | ||
3 | M711BTA1190 | BTA-119 | Al, SST, Nylon, Silicone | LXH | Orthopedic Manual Surgical Instrument | 1 | PSO | |
4 | M711X212163200 | X21216320 | X21216320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
5 | M711X212163000 | X21216300 | X21216300 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
6 | M711X212162800 | X21216280 | X21216280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
7 | M711X212153200 | X21215320 | X21215320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
8 | M711X212153000 | X21215300 | X21215300 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
9 | M711X212152800 | X21215280 | X21215280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
10 | M711X212143200 | X21214320 | X21214320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
11 | M711X212143000 | X21214300 | X21214300 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
12 | M711X212142800 | X21214280 | X21214280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
13 | M711X212133200 | X21213320 | X21213320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
14 | M711X212133000 | X21213300 | X21213300 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
15 | M711X212132800 | X21213280 | X21213280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
16 | M711X212123200 | X21212320 | X21212320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
17 | M711X212123000 | X21212300 | X21212300 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
18 | M711X212122800 | X21212280 | X21212280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
19 | M711X212113200 | X21211320 | X21211320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
20 | M711X212113000 | X21211300 | X21211300 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
21 | M711X212112800 | X21211280 | X21211280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
22 | M711X212103200 | X21210320 | X21210320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
23 | M711X212103000 | X21210300 | X21210300 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
24 | M711X212102800 | X21210280 | X21210280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
25 | M711X212093200 | X21209320 | X21209320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
26 | M711X212093000 | X21209300 | X21209300 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
27 | M711X212092800 | X21209280 | X21209280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
28 | M711X212082800 | X21208280 | X21208280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
29 | M711X210162550 | X21016255 | X21016255 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
30 | M711X210162500 | X21016250 | X21016250 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
31 | M711X210162250 | X21016225 | X21016225 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
32 | M711X210162200 | X21016220 | X21016220 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
33 | M711X210153200 | X21015320 | X21015320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
34 | M711X210152800 | X21015280 | X21015280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
35 | M711X210152550 | X21015255 | X21015255 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
36 | M711X210152500 | X21015250 | X21015250 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
37 | M711X210152250 | X21015225 | X21015225 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
38 | M711X210152200 | X21015220 | X21015220 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
39 | M711X210143200 | X21014320 | X21014320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
40 | M711X210142800 | X21014280 | X21014280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
41 | M711X210142550 | X21014255 | X21014255 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
42 | M711X210142500 | X21014250 | X21014250 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
43 | M711X210142250 | X21014225 | X21014225 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
44 | M711X210142200 | X21014220 | X21014220 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
45 | M711X210133200 | X21013320 | X21013320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
46 | M711X210132800 | X21013280 | X21013280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
47 | M711X210132550 | X21013255 | X21013255 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
48 | M711X210132500 | X21013250 | X21013250 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
49 | M711X210132250 | X21013225 | X21013225 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
50 | M711X210132200 | X21013220 | X21013220 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
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 | 00840180511602 | CI-11084-10-08227010 | LIF Trial, Rasped, 8 X 22 X 70, 10°, Hudson | General Instrument | ALPHATEC SPINE, INC. | |
3 | 00840180511596 | CI-11084-10-06227010 | LIF Trial, Rasped, 6 X 22 X 70, 10°, Hudson | General Instrument | ALPHATEC SPINE, INC. | |
4 | 00840180511589 | CI-11084-10-04227010 | LIF Trial, Rasped, 4 X 22 X 70, 10°, Hudson | General Instrument | ALPHATEC SPINE, INC. | |
5 | 00840180511572 | CI-11084-10-10187010 | LIF Trial, Rasped, 10 X 18 X 70, 10°, Hudson | General Instrument | ALPHATEC SPINE, INC. | |
6 | 00840180511565 | CI-11084-10-08187010 | LIF Trial, Rasped, 8 X 18 X 70, 10°, Hudson | General Instrument | ALPHATEC SPINE, INC. | |
7 | 00840180511558 | CI-11084-10-06187010 | LIF Trial, Rasped, 6 X 18 X 70, 10°, Hudson | General Instrument | ALPHATEC SPINE, INC. | |
8 | 00840180511541 | CI-11084-10-04187010 | LIF Trial, Rasped, 4 X 18 X 70, 10°, Hudson | General Instrument | ALPHATEC SPINE, INC. | |
9 | 00840180511251 | CI-11070-10-12227010 | LIF Trial, 1/3 Rasped, Grooves, 12 x 22 x 70 x 10° | General Instrument | ALPHATEC SPINE, INC. | |
10 | 00840180511244 | CI-11070-10-10227010 | LIF Trial, 1/3 Rasped, Grooves, 10 x 22 x 70 x 10° | General Instrument | ALPHATEC SPINE, INC. | |
11 | 00840180511237 | CI-11070-10-08227010 | LIF Trial, 1/3 Rasped, Grooves, 8 x 22 x 70 x 10° | General Instrument | ALPHATEC SPINE, INC. | |
12 | 00840180511220 | CI-11070-10-06227010 | LIF Trial, 1/3 Rasped, Grooves, 6 x 22 x 70 x 10° | General Instrument | ALPHATEC SPINE, INC. | |
13 | 00840180511213 | CI-11070-10-12187010 | LIF Trial, 1/3 Rasped, Grooves, 12 x 18 x 70 x 10° | General Instrument | ALPHATEC SPINE, INC. | |
14 | 00840180511206 | CI-11070-10-10187010 | LIF Trial, 1/3 Rasped, Grooves, 10 x 18 x 70 x 10° | General Instrument | ALPHATEC SPINE, INC. | |
15 | 00840180511190 | CI-11070-10-08187010 | LIF Trial, 1/3 Rasped, Grooves, 8 x 18 x 70 x 10° | General Instrument | ALPHATEC SPINE, INC. | |
16 | 00840180511183 | CI-11070-10-06187010 | LIF Trial, 1/3 Rasped, Grooves, 6 x 18 x 70 x 10° | General Instrument | ALPHATEC SPINE, INC. | |
17 | 00840180511176 | CI-11070-10-04187010 | LIF Trial, 1/3 Rasped, Grooves, 4 x 18 x 70 x 10° | General Instrument | ALPHATEC SPINE, INC. | |
18 | 00840180510711 | CI-11028 | Cranial Angled Trial Inserter, 15° | General Instrument | ALPHATEC SPINE, INC. | |
19 | 00840180510490 | CI-11024 | Identiti ALIF SA, Squid, Modular Tip | General Instrument | ALPHATEC SPINE, INC. | |
20 | 00840180510438 | CI-10982 | Inserter/Distractor, Squid, Enlarged Slot | General Instrument | ALPHATEC SPINE, INC. | |
21 | 00840180510339 | CI-11003-043828 | ALIF Trial Rasp Template, 4 x 38 x 28mm | General Instrument | ALPHATEC SPINE, INC. | |
22 | 00840180510322 | CI-11003-043424 | ALIF Trial Rasp Template, 4 x 34 x 24mm | General Instrument | ALPHATEC SPINE, INC. | |
23 | 00840180510087 | CI-10982-03 | Modular Inserter Distractor, IdentiTti ALIF Tip | General Instrument | ALPHATEC SPINE, INC. | |
24 | 00840180509999 | CI-10950 | Squid, Distractor Block, 34 x 24 x 10, 7° | General Instrument | ALPHATEC SPINE, INC. | |
25 | 00840180509807 | CI-11010-10-04141207 | Cervical Trial, 4 x 14 x 12, 7° | General Instrument | ALPHATEC SPINE, INC. | |
26 | 00840180509791 | CI-11010-10-04161407 | Cervical Trial, 4 x 16 x 14, 7° | General Instrument | ALPHATEC SPINE, INC. | |
27 | 00840180509784 | CI-11010-10-03161407 | Cervical Trial, 3 x 16 x 14, 7° | General Instrument | ALPHATEC SPINE, INC. | |
28 | 00840180509777 | CI-11010-10-03141207 | Cervical Trial, 3 x 14 x 12, 7° | General Instrument | ALPHATEC SPINE, INC. | |
29 | 00840180508480 | CI-10971-08181607 | Cervical Trial Depth Marker, 18 MM | General Instrument | ALPHATEC SPINE, INC. | |
30 | 00840180508473 | CI-10971-08161407 | Cervical Trial Depth Marker 16 MM | General Instrument | ALPHATEC SPINE, INC. | |
31 | 00840180508466 | CI-10971-08141207 | Cervical Trial Depth Marker 14 mm | General Instrument | ALPHATEC SPINE, INC. | |
32 | 00840180508435 | CI-10972-10-10181607 | U-Shaped Cervical Trial | General Instrument | ALPHATEC SPINE, INC. | |
33 | 00840180506899 | CI-10864-09102515 | IdentiTi PC Trial, 9 x 10 x 25, 15-deg | General Instrument | ALPHATEC SPINE, INC. | |
34 | 00840180506882 | CI-10864-07102515 | IdentiTi PC Trial, 7 x 10 x 25, 15-deg | General Instrument | ALPHATEC SPINE, INC. | |
35 | 00840180506875 | CI-10864-06102515 | IdentiTi PC Trial, 6 x 10 x 25, 15-deg | General Instrument | ALPHATEC SPINE, INC. | |
36 | 00840180505809 | CI-10836 | IdentiTi CV Inserter - 1.5mm Stop | General Instrument | ALPHATEC SPINE, INC. | |
37 | 00840180504864 | CI-10808-02 | Laser Marked PS Inserter Sleeve, 22mm | General Instrument | ALPHATEC SPINE, INC. | |
38 | 00840180504857 | CI-10808-01 | Laser Marker PS Inserter Sleeve | General Instrument | ALPHATEC SPINE, INC. | |
39 | 00840180504826 | CI-10803-10-10227010 | LIF Trial, Rasp, 22 MM, 10P, 10° | General Instrument | ALPHATEC SPINE, INC. | |
40 | 00840180504819 | CI-10803-10-08227010 | LIF Trial, Rasp, 22 MM, 8P, 10° | General Instrument | ALPHATEC SPINE, INC. | |
41 | 00840180504796 | CI-10803-10-06227010 | LIF Trial, Rasp, 22 MM, 6P, 10° | General Instrument | ALPHATEC SPINE, INC. | |
42 | 00840180504772 | CI-10803-10-04227010 | LIF Trial, Rasp, 22 MM, 4P, 10° | General Instrument | ALPHATEC SPINE, INC. | |
43 | 00840180504765 | CI-10803-10-10187010 | LIF Trial, Rasp, 18 MM, 10 MM, 10° | General Instrument | ALPHATEC SPINE, INC. | |
44 | 00840180504758 | CI-10803-10-08187010 | LIF Trial, Rasp, 18 MM, 8MM, 10° | General Instrument | ALPHATEC SPINE, INC. | |
45 | 00840180504741 | CI-10803-10-06187010 | LIF Trial, Rasp, 18 MM, 6MM, 10° | General Instrument | ALPHATEC SPINE, INC. | |
46 | 00840180504734 | CI-10803-10-04187010 | LIF Trial, Rasp, 18 MM, 4 MM, 10° | General Instrument | ALPHATEC SPINE, INC. | |
47 | 00840180504512 | CI-10784-10-10267010 | LIF Trial, Grooved, Straight, 10 x 26 x 70, 10° | General Instrument | ALPHATEC SPINE, INC. | |
48 | 00840180504505 | CI-10784-10-08267010 | LIF Trial, Grooved, Straight, 8 x 26 x 70, 10° | General Instrument | ALPHATEC SPINE, INC. | |
49 | 00840180504499 | CI-10784-10-06267010 | LIF Trial, Grooved, Straight, 6 x 26 x 70 10° | General Instrument | ALPHATEC SPINE, INC. | |
50 | 00840180504475 | CI-10784-10-04267010 | LIF Trial, Grooved, Straight, 4 x 26 x 70 10° | General Instrument | ALPHATEC SPINE, INC. |