No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 00845694041133 | 395-4001-30 | 395-4001-30 | Tag, 0 Degree ExtremiFuse, 3.0 | HWC | Screw, fixation, bone | 2 | OsteoMed |
2 | 00845694041126 | 395-4001-24 | 395-4001-24 | Tag, 0 Degree ExtremiFuse, 2.4 | HWC | Screw, fixation, bone | 2 | OsteoMed |
3 | 00845694041119 | 395-4001-00 | 395-4001-00 | Tag, 0 Degree ExtremiFuse, Blank | HWC | Screw, fixation, bone | 2 | OsteoMed |
4 | 00845694041102 | 395-4000 | 395-4000 | ExtremiFuse Organizer Block | HWC | Screw, fixation, bone | 2 | OsteoMed |
5 | 00845694041096 | 395-2430 | 395-2430 | X-Ray Template, ExtremiFuse | HWC | Screw, fixation, bone | 2 | OsteoMed |
6 | 00845694041089 | 395-2200 | 395-2200 | ExtremiFuse Dual Cannulated Driver Handle | HWC | Screw, fixation, bone | 2 | OsteoMed |
7 | 00845694041072 | 395-2124 | 395-2124 | Broach, ExtremiFuse | HWC | Screw, fixation, bone | 2 | OsteoMed |
8 | 00845694041065 | 395-2027 | 395-2027 | Ø2.7mm Cannulated Drill, Quick Release | HWC | Screw, fixation, bone | 2 | OsteoMed |
9 | 00845694041058 | 395-2000 | 395-2000 | .035 x 3 K-Wire | HWC | Screw, fixation, bone | 2 | OsteoMed |
10 | 00845694041041 | 386-1705 | 386-1705 | Extraction System Tray | KWD | PROSTHESIS, TOE, HEMI-, PHALANGEAL | 2 | OsteoMed |
11 | 00845694041034 | 320-1029 | 320-1029 | Plate Bending Forceps, Large | HRS | Plate, fixation, bone | 2 | OsteoMed |
12 | 00845694041027 | 319-1030 | 319-1030 | 3.0mm x 10 Degree ExtremiFuse Implant | HWC | Screw, fixation, bone | 2 | OsteoMed |
13 | 00845694041010 | 319-1024 | 319-1024 | 2.4mm x 10 Degree ExtremiFuse Implant | HWC | Screw, fixation, bone | 2 | OsteoMed |
14 | 00845694041003 | 319-0030 | 319-0030 | 3.0mm x 0 Degree ExtremiFuse Implant | HWC | Screw, fixation, bone | 2 | OsteoMed |
15 | 00845694040990 | 319-0024 | 319-0024 | 2.4mm x 0 Degree ExtremiFuse Implant | HWC | Screw, fixation, bone | 2 | OsteoMed |
16 | 00845694040969 | 213-0127 | 213-0127 | 1.6mm, Left Zed Plate, 11mm | DZL | SCREW, FIXATION, INTRAOSSEOUS | 2 | OsteoMed |
17 | 00845694040952 | 213-0126 | 213-0126 | 1.6mm, Right Zed Plate, 11mm | DZL | SCREW, FIXATION, INTRAOSSEOUS | 2 | OsteoMed |
18 | 00845694040945 | 210-0255 | 210-0255 | 2.0mm Left L Plate, 23mm, Rigid | DZL | SCREW, FIXATION, INTRAOSSEOUS | 2 | OsteoMed |
19 | 00845694040938 | 210-0254 | 210-0254 | 2.0mm Right L Plate, 23mm, Rigid | DZL | SCREW, FIXATION, INTRAOSSEOUS | 2 | OsteoMed |
20 | 00845694040921 | 210-0253 | 210-0253 | 2.0mm Left L Plate, 18mm, Rigid | DZL | SCREW, FIXATION, INTRAOSSEOUS | 2 | OsteoMed |
21 | 00845694040914 | 210-0252 | 210-0252 | 2.0mm Right L Plate, 18mm, Rigid | DZL | SCREW, FIXATION, INTRAOSSEOUS | 2 | OsteoMed |
22 | 00845694040907 | 210-0251 | 210-0251 | 2.0mm Left L Plate, 15mm, Rigid | DZL | SCREW, FIXATION, INTRAOSSEOUS | 2 | OsteoMed |
23 | 00845694040891 | 210-0250 | 210-0250 | 2.0mm Right L Plate, 15mm, Rigid | DZL | SCREW, FIXATION, INTRAOSSEOUS | 2 | OsteoMed |
24 | 00845694040884 | 211-1606-REV-G | 211-1606-REV-G | 1.6mm x 6mm AUTO-DRIVE Screw | HWC | Screw, fixation, bone | 2 | OsteoMed |
25 | 00845694040877 | 213-0018-SP | 213-0018-SP | 1.6mm Rigid Curved Plate, 10 Hole, Sterile | DZL | SCREW, FIXATION, INTRAOSSEOUS | 2 | OsteoMed |
26 | 00845694040860 | 212-0052-SP | 212-0052-SP | 19mm T Plate, Sterile | JEY | PLATE, BONE | 2 | OsteoMed |
27 | 00845694040853 | 212-0046-SP | 212-0046-SP | 13mm Right L Plate, Sterile | JEY | PLATE, BONE | 2 | OsteoMed |
28 | 00845694040846 | 212-0044-SP | 212-0044-SP | 13mm Left L Plate, Sterile | JEY | PLATE, BONE | 2 | OsteoMed |
29 | 00845694040839 | 212-0030-SP | 212-0030-SP | 7 Hole Y Plate, Sterile | DZL | SCREW, FIXATION, INTRAOSSEOUS | 2 | OsteoMed |
30 | 00845694040822 | 213-0011-SP | 213-0011-SP | 10 Hole Curved Plate, Sterile | DZL | SCREW, FIXATION, INTRAOSSEOUS | 2 | OsteoMed |
31 | 00845694040815 | 817-1017 | 817-1017 | PrimaLIF LLIF 17mm x 26mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
32 | 00845694040808 | 817-1015 | 817-1015 | PrimaLIF LLIF 15mm x 26mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
33 | 00845694040792 | 817-1013 | 817-1013 | PrimaLIF LLIF 13mm x 26mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
34 | 00845694040785 | 817-1011 | 817-1011 | PrimaLIF LLIF 11mm x 26mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
35 | 00845694040778 | 817-1009 | 817-1009 | PrimaLIF LLIF 9mm x 26mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
36 | 00845694040761 | 817-1007 | 817-1007 | PrimaLIF LLIF 7mm x 26mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
37 | 00845694040754 | 816-1017 | 816-1017 | PrimaLIF LLIF 17mm x 22mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
38 | 00845694040747 | 816-1015 | 816-1015 | PrimaLIF LLIF 15mm x 22mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
39 | 00845694040730 | 816-1013 | 816-1013 | PrimaLIF LLIF 13mm x 22mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
40 | 00845694040723 | 816-1011 | 816-1011 | PrimaLIF LLIF 11mm x 22mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
41 | 00845694040716 | 816-1009 | 816-1009 | PrimaLIF LLIF 9mm x 22mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
42 | 00845694040709 | 816-1007 | 816-1007 | PrimaLIF LLIF 7mm x 22mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
43 | 00845694040693 | 815-1017 | 815-1017 | PrimaLIF LLIF 17mm x 18mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
44 | 00845694040686 | 815-1015 | 815-1015 | PrimaLIF LLIF 15mm x 18mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
45 | 00845694040679 | 815-1013 | 815-1013 | PrimaLIF LLIF 13mm x 18mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
46 | 00845694040662 | 815-1011 | 815-1011 | PrimaLIF LLIF 11mm x 18mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
47 | 00845694040655 | 815-1009 | 815-1009 | PrimaLIF LLIF 9mm x 18mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
48 | 00845694040648 | 815-1007 | 815-1007 | PrimaLIF LLIF 7mm x 18mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
49 | 00845694040631 | 814-1017 | 814-1017 | PrimaLIF LLIF 17mm x 26mm Parallel Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
50 | 00845694040624 | 814-1015 | 814-1015 | PrimaLIF LLIF 15mm x 26mm Parallel Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 07613327004021 | 78-10020 | 78-10020 | PEEK CUSTOMIZED CRANIAL IMPLANT KIT, M | NA | STRYKER LEIBINGER GMBH & CO. KG |
2 | 07613252660743 | 92-00692 | 92-00692 | Mesh Plate, round, small | UNIVERSAL NEURO 3 | STRYKER LEIBINGER GMBH & CO. KG |
3 | 07613252660736 | 92-00664 | 92-00664 | Mesh Plate, round, medium | NA | STRYKER LEIBINGER GMBH & CO. KG |
4 | 07613252660729 | 92-00666 | 92-00666 | Mesh Plate, round, large | UNIVERSAL NEURO 3 | STRYKER LEIBINGER GMBH & CO. KG |
5 | 07613252660712 | 92-00486 | 92-00486 | Suboccipital Plate, large | UNIVERSAL NEURO 3 | STRYKER LEIBINGER GMBH & CO. KG |
6 | 07613252471547 | 92-34228 | 92-34228 | BOX PLATE, SMALL | UNIVERSAL NEURO 3 | STRYKER LEIBINGER GMBH & CO. KG |
7 | 07613252288220 | 12-01536S | 12-01536S | 2 H. PLATES(2) 20mm BHC(1) SD SCREW(10) | NA | STRYKER LEIBINGER GMBH & CO. KG |
8 | 07613252288213 | 12-01534S | 12-01534S | 2 H. PLATES(2) 14mm BHC(1) SD SCREW(10) | NA | STRYKER LEIBINGER GMBH & CO. KG |
9 | 07613252288206 | 12-01532S | 12-01532S | 2 HOLE PLATES W/TAB(3) LP SD SCREW(6) | NA | STRYKER LEIBINGER GMBH & CO. KG |
10 | 07613252288190 | 12-01530S | 12-01530S | 2 HOLE PLATES(3) SELF DRILLING SCREW(6) | NA | STRYKER LEIBINGER GMBH & CO. KG |
11 | 07613252288183 | 12-01531S | 12-01531S | 2 HOLE PLATES(3) SELF TAPPING SCREW(6) | NA | STRYKER LEIBINGER GMBH & CO. KG |
12 | 04546540730800 | 78-10100 | 78-10100 | PEEK CUSTOMIZED CRANIOFACIAL IMPLANT KIT | NA | STRYKER LEIBINGER GMBH & CO. KG |
13 | 04546540730794 | 78-10040 | 78-10040 | PEEK CUSTOMIZED CRANIAL IMPLANT KIT, XL | NA | STRYKER LEIBINGER GMBH & CO. KG |
14 | 04546540730787 | 78-10030 | 78-10030 | PEEK CUSTOMIZED CRANIAL IMPLANT KIT, L | NA | STRYKER LEIBINGER GMBH & CO. KG |
15 | 04546540730763 | 78-10010 | 78-10010 | PEEK CUSTOMIZED CRANIAL IMPLANT KIT, S | NA | STRYKER LEIBINGER GMBH & CO. KG |
16 | 04546540684851 | 53-36212 | 53-36212 | Straight Plate, 12mm Bar | UNIVERSAL NEURO 3 | STRYKER LEIBINGER GMBH & CO. KG |
17 | 04546540684844 | 53-34804 | 53-34804 | Straight Plate | UNIVERSAL NEURO 3 | STRYKER LEIBINGER GMBH & CO. KG |
18 | 04546540684837 | 53-34630 | 53-34630 | X Plate | UNIVERSAL NEURO 3 | STRYKER LEIBINGER GMBH & CO. KG |
19 | 04546540684820 | 53-34622 | 53-34622 | Gap Plate, large | UNIVERSAL NEURO 3 | STRYKER LEIBINGER GMBH & CO. KG |
20 | 04546540684790 | 53-34612 | 53-34612 | Gap Plate, small | UNIVERSAL NEURO 3 | STRYKER LEIBINGER GMBH & CO. KG |
21 | 04546540684783 | 53-34608 | 53-34608 | Double-Y Plate | UNIVERSAL NEURO 3 | STRYKER LEIBINGER GMBH & CO. KG |
22 | 04546540684721 | 53-34406 | 53-34406 | Straight Plate, 6mm Bar | UNIVERSAL NEURO 3 | STRYKER LEIBINGER GMBH & CO. KG |
23 | 04546540684714 | 53-34300 | 53-34300 | Rectangle Plate | UNIVERSAL NEURO 3 | STRYKER LEIBINGER GMBH & CO. KG |
24 | 04546540684707 | 53-34240 | 53-34240 | Box Plate, large | UNIVERSAL NEURO 3 | STRYKER LEIBINGER GMBH & CO. KG |
25 | 04546540684691 | 53-34230 | 53-34230 | Box Plate, large, with Tab | UNIVERSAL NEURO 3 | STRYKER LEIBINGER GMBH & CO. KG |
26 | 04546540684684 | 53-34228 | 53-34228 | Box Plate, small | UNIVERSAL NEURO 3 | STRYKER LEIBINGER GMBH & CO. KG |
27 | 04546540684677 | 53-34216 | 53-34216 | Straight Plate, 16mm Bar | UNIVERSAL NEURO 3 | STRYKER LEIBINGER GMBH & CO. KG |
28 | 04546540684660 | 53-34212 | 53-34212 | Straight Plate, 12mm Bar, with Tab | UNIVERSAL NEURO 3 | STRYKER LEIBINGER GMBH & CO. KG |
29 | 04546540684653 | 53-34164 | 53-34164 | Straight Plate | UNIVERSAL NEURO 3 | STRYKER LEIBINGER GMBH & CO. KG |
30 | 04546540684646 | 53-00486 | 53-00486 | Suboccipital Plate, large | UNIVERSAL NEURO 3 | STRYKER LEIBINGER GMBH & CO. KG |
31 | 04546540684639 | 53-00466 | 53-00466 | Mesh Plate, round, large | UNIVERSAL NEURO 3 | STRYKER LEIBINGER GMBH & CO. KG |
32 | 04546540684622 | 53-00382 | 53-00382 | Suboccipital Plate, small | UNIVERSAL NEURO 3 | STRYKER LEIBINGER GMBH & CO. KG |
33 | 04546540684615 | 53-00364 | 53-00364 | Mesh Plate, round, medium | NA | STRYKER LEIBINGER GMBH & CO. KG |
34 | 04546540684608 | 53-00362 | 53-00362 | Mesh Plate, round, small | UNIVERSAL NEURO 3 | STRYKER LEIBINGER GMBH & CO. KG |
35 | 04546540684592 | 53-00346 | 53-00346 | Translabyrinthine Plate, large | UNIVERSAL NEURO 3 | STRYKER LEIBINGER GMBH & CO. KG |
36 | 04546540684585 | 53-00342 | 53-00342 | Translabyrinthine Plate, small | UNIVERSAL NEURO 3 | STRYKER LEIBINGER GMBH & CO. KG |
37 | 04546540684578 | 53-00324 | 53-00324 | Temporal Plate, medium | UNIVERSAL NEURO 3 | STRYKER LEIBINGER GMBH & CO. KG |
38 | G28441001 | 410-01 | The NeuroVention Cranial Fixation System is intended for use as a burr hole cove The NeuroVention Cranial Fixation System is intended for use as a burr hole cover and/or skull bone fixation followingcraniotomy, cranioplasty, or craniectomy surgery. KTC 3-piece plate is made from PEEK. | KTC Burr Hole Cover | NEUROVENTION LLC | |
39 | G28440901 | 409-01 | The NeuroVention Cranial Fixation System is intended for use as a burr hole cove The NeuroVention Cranial Fixation System is intended for use as a burr hole cover and/or skull bone fixation following craniotomy, cranioplasty, or craniectomy surgery. KTC 2-piece plate is made from PEEK . | KTC Burr Hole Cover | NEUROVENTION LLC | |
40 | G28436102 | 361-02 | The NeuroVention Cranial Fixation System is intended for use as a burr hole cove The NeuroVention Cranial Fixation System is intended for use as a burr hole cover and/or skull bone fixation followingcraniotomy, cranioplasty, or craniectomy surgery. | NuCrani Large Plate | NEUROVENTION LLC | |
41 | G28433001 | 330-01 | The NeuroVention Cranial Fixation System is intended for use as a burr hole cove The NeuroVention Cranial Fixation System is intended for use as a burr hole cover and/or skull bone fixation followingcraniotomy, cranioplasty, or craniectomy surgery. | NuCrani Small Plate | NEUROVENTION LLC | |
42 | 00898142001944 | 16-1P3-3867 | 16-1P3-3867 | Plate Panel, 0.4mm x 38mm x 67mm | NeuroPro® Low Profile | KINAMED, INC. |
43 | 00898142001920 | 16-1P1-1480 | 16-1P1-1480 | Straight, 14 Hole Plate, 77mm Plate | NeuroPro® Low Profile | KINAMED, INC. |
44 | 00898142001746 | 16-1P3-9013 | 16-1P3-9013 | Hex Panel, 0.2mm x 90mm x 135mm | NeuroPro® Low Profile | KINAMED, INC. |
45 | 00898142001739 | 16-1P3-4066 | 16-1P3-4066 | Hex Panel, 0.2mm x 40mm x 66mm | NeuroPro® Low Profile | KINAMED, INC. |
46 | 00898142001722 | 16-1P3-3869 | 16-1P3-3869 | Plate Panel, 0.6mm x 38mm x 67mm | NeuroPro® Low Profile | KINAMED, INC. |
47 | 00898142001708 | 16-1P3-8915 | 16-1P3-8915 | Plate Panel, 0.6mm x 89mm x 135mm | NeuroPro® Low Profile | KINAMED, INC. |
48 | 00898142001692 | 16-1P3-8913 | 16-1P3-8913 | Plate Panel, 0.4mm x 89mm x 135mm | NeuroPro® Low Profile | KINAMED, INC. |
49 | 00898142001685 | 16-1P3-1045 | 16-1P3-1045 | Gap Panel, 0.25mm x 10mm x 45mm | NeuroPro® Low Profile | KINAMED, INC. |
50 | 00898142001623 | 16-1P1-3183 | 16-1P1-3183 | Straight, 31 Hole, 183mm Plate | NeuroPro® Low Profile | KINAMED, INC. |