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 | 00844856099173 | 25600-318-S | ALPHATEC SOLUS LUMBAR SPACER, 18mm LARGE, 12 LORDOTIC, STERILE | ALPHATEC SOLUS | ALPHATEC SPINE, INC. | |
2 | 00844856099166 | 25600-316-S | ALPHATEC SOLUS LUMBAR SPACER, 16mm LARGE, 12 LORDOTIC, STERILE | ALPHATEC SOLUS | ALPHATEC SPINE, INC. | |
3 | 00844856099159 | 25600-314-S | ALPHATEC SOLUS LUMBAR SPACER, 14mm LARGE, 12 LORDOTIC, STERILE | ALPHATEC SOLUS | ALPHATEC SPINE, INC. | |
4 | 00844856099142 | 25600-312-S | ALPHATEC SOLUS LUMBAR SPACER, 12mm LARGE, 12 LORDOTIC, STERILE | ALPHATEC SOLUS | ALPHATEC SPINE, INC. | |
5 | 00844856099135 | 25600-118-S | ALPHATEC SOLUS LUMBAR SPACER, 18mm LARGE, 7 LORDOTIC, STERILE | ALPHATEC SOLUS | ALPHATEC SPINE, INC. | |
6 | 00844856099128 | 25600-116-S | ALPHATEC SOLUS LUMBAR SPACER, 16mm LARGE, 7 LORDOTIC, STERILE | ALPHATEC SOLUS | ALPHATEC SPINE, INC. | |
7 | 00844856099111 | 25600-114-S | ALPHATEC SOLUS LUMBAR SPACER, 14mm LARGE, 7 LORDOTIC, STERILE | ALPHATEC SOLUS | ALPHATEC SPINE, INC. | |
8 | 00844856099104 | 25600-112-S | ALPHATEC SOLUS LUMBAR SPACER, 12mm LARGE, 7 LORDOTIC, STERILE | ALPHATEC SOLUS | ALPHATEC SPINE, INC. | |
9 | 00844856099098 | 25600-110-S | ALPHATEC SOLUS LUMBAR SPACER, 10mm LARGE, 7 LORDOTIC, STERILE | ALPHATEC SOLUS | ALPHATEC SPINE, INC. | |
10 | 00844856099081 | 25200-316-S | ALPHATEC SOLUS LUMBAR SPACER, 16mm MEDIUM, 12 LORDOTIC, STERILE | ALPHATEC SOLUS | ALPHATEC SPINE, INC. | |
11 | 00844856099074 | 25200-314-S | ALPHATEC SOLUS LUMBAR SPACER, 14mm MEDIUM, 12 LORDOTIC, STERILE | ALPHATEC SOLUS | ALPHATEC SPINE, INC. | |
12 | 00844856099067 | 25200-312-S | ALPHATEC SOLUS LUMBAR SPACER, 12mm MEDIUM, 12 LORDOTIC, STERILE | ALPHATEC SOLUS | ALPHATEC SPINE, INC. | |
13 | 00844856099050 | 25200-116-S | ALPHATEC SOLUS LUMBAR SPACER, 16mm MEDIUM, 7 LORDOTIC, STERILE | ALPHATEC SOLUS | ALPHATEC SPINE, INC. | |
14 | 00844856099043 | 25200-114-S | ALPHATEC SOLUS LUMBAR SPACER, 14mm MEDIUM, 7 LORDOTIC, STERILE | ALPHATEC SOLUS | ALPHATEC SPINE, INC. | |
15 | 00844856099036 | 25200-112-S | ALPHATEC SOLUS LUMBAR SPACER, 12mm MEDIUM, 7 LORDOTIC, STERILE | ALPHATEC SOLUS | ALPHATEC SPINE, INC. | |
16 | 00844856099029 | 25200-110-S | ALPHATEC SOLUS LUMBAR SPACER, 10mm MEDIUM, 7 LORDOTIC, STERILE | ALPHATEC SOLUS | ALPHATEC SPINE, INC. | |
17 | 00844856054387 | 25910 | Solus Lumbar Inserter / Distractor | Alphatec Solus | ALPHATEC SPINE, INC. | |
18 | 00843193111661 | M391716c-35 | M391716c-35 | MIDLINE II-Ti | CENTINEL SPINE, INC. | |
19 | 00843193111654 | M391516c-35 | M391516c-35 | MIDLINE II-Ti | CENTINEL SPINE, INC. | |
20 | 00843193111647 | M391512c-35 | M391512c-35 | MIDLINE II-Ti | CENTINEL SPINE, INC. | |
21 | 00843193111630 | M391312c-35 | M391312c-35 | MIDLINE II-Ti | CENTINEL SPINE, INC. | |
22 | 00843193111623 | M391508c-35 | M391508c-35 | MIDLINE II-Ti | CENTINEL SPINE, INC. | |
23 | 00843193111616 | M391308c-35 | M391308c-35 | MIDLINE II-Ti | CENTINEL SPINE, INC. | |
24 | 00843193111609 | M361512c-32 | M361512c-32 | MIDLINE II-Ti | CENTINEL SPINE, INC. | |
25 | 00843193111593 | M361312c-32 | M361312c-32 | MIDLINE II-Ti | CENTINEL SPINE, INC. | |
26 | 00843193111586 | M361508c-32 | M361508c-32 | MIDLINE II-Ti | CENTINEL SPINE, INC. | |
27 | 00843193111579 | M361308c-32 | M361308c-32 | MIDLINE II-Ti | CENTINEL SPINE, INC. | |
28 | 00842166195264 | 0100123 5660-400-001 | Tertiary Instrument Case 26mm Sizers - Assembly | Zavation | ZAVATION LLC | |
29 | 00842166195257 | 0100009 5488-400-001 | Primary Instrument Case 0 deg - Assembly | Zavation | ZAVATION LLC | |
30 | 00842166195240 | 0100004 5487-400-001 | Primary Instrument Case 6 deg - Assembly | Zavation | ZAVATION LLC | |
31 | 00842166195233 | 0100067 5490-400-001 | Disc Prep Case 2 Assembly | Zavation | ZAVATION LLC | |
32 | 00842166195226 | 0100058 5489-400-001 | Disc Prep Case 1 Assembly | Zavation | ZAVATION LLC | |
33 | 00842166195219 | 0100005 | Generic Sterilization Lid | Zavation | ZAVATION LLC | |
34 | 00842166195189 | 470-9003 | MILC 6 Degree Cage Case | Zavation | ZAVATION LLC | |
35 | 00842166195172 | 470-9002 | MILC 0 Degree Cage Case | Zavation | ZAVATION LLC | |
36 | 00842166195165 | 470-9001 | MILC Plate and Screw Case | Zavation | ZAVATION LLC | |
37 | 00842166195073 | 210-9000 | Z-Direct Instrument Tray | Zavation | ZAVATION LLC | |
38 | 00842166195028 | 180-9000 | Z-Link Lumbar Tray | Zavation | ZAVATION LLC | |
39 | 00842166191877 | ZAV-1260 | Custom T15 E-Split Tipped Universal Driver | Zavation | ZAVATION LLC | |
40 | 00842166191860 | ZAV-1258 | Custom T15 e-Split Tipped Driver | Zavation | ZAVATION LLC | |
41 | 00842166189218 | 473-1235-4 | Ferris Smith Pituitary 12” with Special Trigger Handle Angled 15° Left | ZAVATION | ZAVATION LLC | |
42 | 00842166189201 | 473-1233-4 | Ferris Smith Pituitary 12” with Special Trigger Handle Angled 15° Left | ZAVATION | ZAVATION LLC | |
43 | 00842166189195 | 473-1235-3 | Ferris Smith Pituitary 12” with Special Trigger Handle Angled 15° Right | ZAVATION | ZAVATION LLC | |
44 | 00842166189188 | 473-1233-3 | Ferris Smith Pituitary 12” with Special Trigger Handle Angled 15° Right | ZAVATION | ZAVATION LLC | |
45 | 00842166189171 | 473-1205-1 | Kerrison Rongeur 12” 90° Up Biting | ZAVATION | ZAVATION LLC | |
46 | 00842166189164 | 473-1203-1 | Kerrison Rongeur 12” 90° Up Biting | ZAVATION | ZAVATION LLC | |
47 | 00842166189157 | 473-1205-0 | 12” Kerrison Rongeur 40° FWD | ZAVATION | ZAVATION LLC | |
48 | 00842166189140 | 473-1203-0 | 12” Kerrison Rongeur 40° FWD | ZAVATION | ZAVATION LLC | |
49 | 00842166189133 | 473-0008-1-9 | 8FR Frazier Suction Tube 9” From the Bend | ZAVATION | ZAVATION LLC | |
50 | 00842166189126 | 472-0014-12 | Custom Angled Bayonet Triangle Endplate Scraper | ZAVATION | ZAVATION LLC |