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 | 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 | |
2 | 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 | |
3 | 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 | |
4 | 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 | |
5 | 00898142001944 | 16-1P3-3867 | 16-1P3-3867 | Plate Panel, 0.4mm x 38mm x 67mm | NeuroPro® Low Profile | KINAMED, INC. |
6 | 00898142001920 | 16-1P1-1480 | 16-1P1-1480 | Straight, 14 Hole Plate, 77mm Plate | NeuroPro® Low Profile | KINAMED, INC. |
7 | 00898142001746 | 16-1P3-9013 | 16-1P3-9013 | Hex Panel, 0.2mm x 90mm x 135mm | NeuroPro® Low Profile | KINAMED, INC. |
8 | 00898142001739 | 16-1P3-4066 | 16-1P3-4066 | Hex Panel, 0.2mm x 40mm x 66mm | NeuroPro® Low Profile | KINAMED, INC. |
9 | 00898142001722 | 16-1P3-3869 | 16-1P3-3869 | Plate Panel, 0.6mm x 38mm x 67mm | NeuroPro® Low Profile | KINAMED, INC. |
10 | 00898142001708 | 16-1P3-8915 | 16-1P3-8915 | Plate Panel, 0.6mm x 89mm x 135mm | NeuroPro® Low Profile | KINAMED, INC. |
11 | 00898142001692 | 16-1P3-8913 | 16-1P3-8913 | Plate Panel, 0.4mm x 89mm x 135mm | NeuroPro® Low Profile | KINAMED, INC. |
12 | 00898142001685 | 16-1P3-1045 | 16-1P3-1045 | Gap Panel, 0.25mm x 10mm x 45mm | NeuroPro® Low Profile | KINAMED, INC. |
13 | 00898142001623 | 16-1P1-3183 | 16-1P1-3183 | Straight, 31 Hole, 183mm Plate | NeuroPro® Low Profile | KINAMED, INC. |
14 | 00898142001616 | 16-1P1-0812 | 16-1P1-0812 | Box Shape, 4 Hole Plate | NeuroPro® Low Profile | KINAMED, INC. |
15 | 00898142001609 | 16-1P1-0810 | 16-1P1-0810 | "X", 4 Hole Plate | NeuroPro® Low Profile | KINAMED, INC. |
16 | 00898142001593 | 16-1P1-0612 | 16-1P1-0612 | "H", 4 Hole Plate | NeuroPro® Low Profile | KINAMED, INC. |
17 | 00898142001586 | 16-1P1-0413 | 16-1P1-0413 | "T", 5 Hole Plate | NeuroPro® Low Profile | KINAMED, INC. |
18 | 00898142001579 | 16-1P1-0214 | 16-1P1-0214 | Straight, wide, 2 Hole Plate | NeuroPro® Low Profile | KINAMED, INC. |
19 | 00898142001562 | 16-1P1-0211 | 16-1P1-0211 | Straight 2 Hole Plate, 11mm | NeuroPro® Low Profile | KINAMED, INC. |
20 | 00888233025324 | 91-6804-EA | 91-6804-EA | THINFLAP SYSTEM | BIOMET MICROFIXATION, INC | |
21 | 00888233025317 | 91-6804-5PK | 91-6804-5PK | THINFLAP SYSTEM 5/PK | BIOMET MICROFIXATION, INC | |
22 | 00888233024648 | 01-7347-5PK | 01-7347-5PK | 1.5MM SYSTEM 5-PACK | BIOMET MICROFIXATION, INC | |
23 | 00888233024631 | 01-7345-5PK | 01-7345-5PK | 1.5MM SYSTEM | BIOMET MICROFIXATION, INC | |
24 | 00888233024624 | 01-7112-5PK | 01-7112-5PK | 1.5MM SYSTEM | BIOMET MICROFIXATION, INC | |
25 | 00888233024617 | 01-7104-5PK | 01-7104-5PK | 1.5MM SYSTEM | BIOMET MICROFIXATION, INC | |
26 | 00888233024600 | 01-7048-5PK | 01-7048-5PK | 1.5MM SYSTEM | BIOMET MICROFIXATION, INC | |
27 | 00888233022330 | SP-3132 | SP-3132 | 1.5MM SYSTEM | BIOMET MICROFIXATION, INC | |
28 | 00888233021876 | SP-3089 | SP-3089 | N/A | BIOMET MICROFIXATION, INC | |
29 | 00888233021562 | SP-3039 | SP-3039 | 1.5MM SYSTEM | BIOMET MICROFIXATION, INC | |
30 | 00888233021555 | SP-3038 | SP-3038 | THINFLAP SYSTEM | BIOMET MICROFIXATION, INC | |
31 | 00888233021517 | SP-3033 | SP-3033 | 1.5MM SYSTEM | BIOMET MICROFIXATION, INC | |
32 | 00888233021432 | SP-3023 | SP-3023 | 1.5MM SYSTEM | BIOMET MICROFIXATION, INC | |
33 | 00888233021418 | SP-3021 | SP-3021 | 1.5MM SYSTEM | BIOMET MICROFIXATION, INC | |
34 | 00888233021357 | SP-3014 | SP-3014 | 1.5MM SYSTEM | BIOMET MICROFIXATION, INC | |
35 | 00888233021302 | SP-3002 | SP-3002 | 1.5MM SYSTEM | BIOMET MICROFIXATION, INC | |
36 | 00888233020527 | SP-2929 | SP-2929 | 1.5MM SYSTEM | BIOMET MICROFIXATION, INC | |
37 | 00888233020503 | SP-2928 | SP-2928 | 1.5MM SYSTEM | BIOMET MICROFIXATION, INC | |
38 | 00888233020442 | SP-2923 | SP-2923 | 1.5MM SYSTEM | BIOMET MICROFIXATION, INC | |
39 | 00888233020428 | SP-2922 | SP-2922 | 1.5MM SYSTEM | BIOMET MICROFIXATION, INC | |
40 | 00888233020404 | SP-2921 | SP-2921 | 1.5MM SYSTEM | BIOMET MICROFIXATION, INC | |
41 | 00888233020145 | SP-2906 | SP-2906 | 1.5MM SYSTEM | BIOMET MICROFIXATION, INC | |
42 | 00888233020121 | SP-2905 | SP-2905 | 1.5MM SYSTEM | BIOMET MICROFIXATION, INC | |
43 | 00888233020091 | SP-2904 | SP-2904 | 1.5MM SYSTEM | BIOMET MICROFIXATION, INC | |
44 | 00888233019989 | SP-2892 | SP-2892 | 1.5MM SYSTEM | BIOMET MICROFIXATION, INC | |
45 | 00888233019880 | SP-2888 | SP-2888 | 1.5MM SYSTEM | BIOMET MICROFIXATION, INC | |
46 | 00888233019866 | SP-2887 | SP-2887 | 1.5MM SYSTEM | BIOMET MICROFIXATION, INC | |
47 | 00888233019842 | SP-2886 | SP-2886 | 1.5MM SYSTEM | BIOMET MICROFIXATION, INC | |
48 | 00888233019828 | SP-2885 | SP-2885 | 1.5MM SYTEM | BIOMET MICROFIXATION, INC | |
49 | 00888233019804 | SP-2884 | SP-2884 | 1.5MM SYSTEM | BIOMET MICROFIXATION, INC | |
50 | 00888233019781 | SP-2883 | SP-2883 | 1.5MM SYSTEM | BIOMET MICROFIXATION, INC |