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 | 00850017962613 | 10-0010 | 10-0010 | 10mm x 8mm Drill | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
2 | 00850017962606 | 10-0210 | 10-0210 | 10mm x 14mm Drill, Long | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
3 | 00850017962590 | 40-1014-01 | 40-1014-01 | HA Coated 10 mm x 14 mm S-Core™ Implant W/Delivery system (00850017962583 and 00 HA Coated 10 mm x 14 mm S-Core™ Implant W/Delivery system (00850017962583 and 00850017962439) | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
4 | 00850017962583 | 10-2014-S | 10-2014-S | 10 mm x 14 mm Cannulated Drill Long and 10 mm Countersink (00850017962606 and 00 10 mm x 14 mm Cannulated Drill Long and 10 mm Countersink (00850017962606 and 00850017962576) | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
5 | 00850017962569 | 10-1090 | 10-1090 | 9mm Countersink | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
6 | 00850017962552 | 10-1080 | 10-1080 | 8mm Countersink | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
7 | 00850017962545 | 10-1070 | 10-1070 | 6mm Countersink | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
8 | 00850017962538 | 10-1060 | 10-1060 | 6mm Countersink | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
9 | 00850017962521 | 10-1050 | 10-1050 | 5mm Countersink | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
10 | 00850017962514 | 10-1040 | 10-1040 | 4mm Countersink | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
11 | 00850017962507 | 10-0009 | 10-0009 | 9mm x 7.5mm Drill | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
12 | 00850017962491 | 10-0008 | 10-0008 | 8mm x 7mm Drill | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
13 | 00850017962477 | 10-0006 | 10-0006 | 6mm x 6mm Drill | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
14 | 00850017962460 | 10-0005 | 10-0005 | 5mm x 5.5mm Drill | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
15 | 00850017962453 | 10-0004 | 10-0004 | 4mm x 5mm Drill | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
16 | 00850017962446 | 10-1100 | 10-1100 | Cannulated Sizer Set (00850017962354, 00850017962361, 00850017962378, 0085001796 Cannulated Sizer Set (00850017962354, 00850017962361, 00850017962378, 00850017962385, 00850017962392, 00850017962408, 00850017962415, 00850017962422, 008500179624239) | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
17 | 00850017962439 | 20-1014-01 | 20-1014-01 | HA Coated 10 mm x 14 mm S-Core™ Implant | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
18 | 00850017962422 | 10-4010 | 10-4010 | T10 Torque Driver | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
19 | 00850017962415 | 10-1145 | 10-1145 | Size 4 Cannulated Sizer | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
20 | 00850017962408 | 10-1155 | 10-1155 | Size 5 Cannulated Sizer | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
21 | 00850017962392 | 10-1165 | 10-1165 | Size 6 Cannulated Sizer | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
22 | 00850017962385 | 10-1175 | 10-1175 | Size 7 Cannulated Sizer | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
23 | 00850017962378 | 10-1185 | 10-1185 | Size 8 Cannulated Sizer | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
24 | 00850017962361 | 10-1195 | 10-1195 | Size 9 Cannulated Sizer | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
25 | 00850017962354 | 10-1105 | 10-1105 | Size 10 Cannulated Sizer | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
26 | 00850017962347 | 40-1000-01 | 40-1000-01 | HA Coated 10 mm x 10 mm S-Core™ Implant W/Delivery system (00850017962200 and 00 HA Coated 10 mm x 10 mm S-Core™ Implant W/Delivery system (00850017962200 and 00850017962279) | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
27 | 00850017962330 | 40-0900-01 | 40-0900-01 | HA Coated 9 mm x 9.5 mm S-Core™ Implant W/Delivery system (00850017962194 and 00 HA Coated 9 mm x 9.5 mm S-Core™ Implant W/Delivery system (00850017962194 and 00850017962262) | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
28 | 00850017962323 | 40-0800-01 | 40-0800-01 | HA Coated 8 mm x 9 mm S-Core™ Implant W/Delivery system (00850017962187 and 0085 HA Coated 8 mm x 9 mm S-Core™ Implant W/Delivery system (00850017962187 and 00850017962255) | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
29 | 00850017962316 | 40-0700-01 | 40-0700-01 | HA Coated 7 mm x 8.5 mm S-Core™ Implant W/Delivery system (00850017962170 and 00 HA Coated 7 mm x 8.5 mm S-Core™ Implant W/Delivery system (00850017962170 and 00850017962248) | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
30 | 00850017962309 | 40-0600-01 | 40-0600-01 | HA Coated 6 mm x 8 mm S-Core™ Implant W/Delivery system (00850017962163 and 0085 HA Coated 6 mm x 8 mm S-Core™ Implant W/Delivery system (00850017962163 and 00850017962231) | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
31 | 00850017962293 | 40-0500-01 | 40-0500-01 | HA Coated 5 mm x 7.5 mm S-Core™ Implant W/Delivery system (00850017962156 and 00 HA Coated 5 mm x 7.5 mm S-Core™ Implant W/Delivery system (00850017962156 and 00850017962224) | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
32 | 00850017962286 | 40-0400-01 | 40-0400-01 | HA Coated 4 mm x 7 mm S-Core™ Implant W/Delivery system (00850017962149 and 0085 HA Coated 4 mm x 7 mm S-Core™ Implant W/Delivery system (00850017962149 and 00850017962217) | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
33 | 00850017962279 | 10-2010-S | 10-2010-S | 10 mm x 8 mm Cannulated Drill and 10 mm Countersink (00850017962576 and 00850017962613) | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
34 | 00850017962262 | 10-2009-S | 10-2009-S | 9 mm x 7.5 mm Cannulated Drill and 9 mm Countersink (00850017962569 and 00850017962507) | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
35 | 00850017962255 | 10-2008-S | 10-2008-S | 8 mm x 7 mm Cannulated Drill and 8 mm Countersink (00850017962552 and 00850017962491) | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
36 | 00850017962248 | 10-2007-S | 10-2007-S | 7 mm x 6.5 mm Cannulated Drill and 7 mm Countersink (00850017962545 and 00850017962484) | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
37 | 00850017962231 | 10-2006-S | 10-2006-S | 6 mm x 6 mm Cannulated Drill and 6 mm Countersink (00850017962538 and 00850017962477) | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
38 | 00850017962224 | 10-2005-S | 10-2005-S | 5 mm x 5.5 mm Cannulated Drill and 5 mm Countersink (00850017962521 and 00850017962460) | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
39 | 00850017962217 | 10-2004-S | 10-2004-S | 4 mm x 5mm Cannulated Drill and 4 mm Countersink (00850017962514 and 00850017962453) | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
40 | 00850017962200 | 20-1000-01-P | 20-1000-01-P | HA Coated 10 mm x 10 mm S-Core Implant | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
41 | 00850017962194 | 20-0900-01-P | 20-0900-01-P | HA Coated 9 mm x 9.5 mm S-Core Implant | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
42 | 00850017962187 | 20-0800-01-P | 20-0800-01-P | HA Coated 8 mm x 9 mm S-Core Implant | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
43 | 00850017962170 | 20-0700-01-P | 20-0700-01-P | HA Coated 7 mm x 8.5 mm S-Core Implant | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
44 | 00850017962163 | 20-0600-01-P | 20-0600-01-P | HA Coated 6 mm x 8 mm S-Core Implant | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
45 | 00850017962156 | 20-0500-01-P | 20-0500-01-P | HA Coated 5 mm x 7.5 mm S-Core Implant | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
46 | 00850017962149 | 20-0400-01-P | 20-0400-01-P | HA Coated 4 mm x 7 mm S-Core Implant | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
47 | 00850017962132 | 10-2010-P | 10-2010-P | 10 mm x 8 mm Cannulated Drill and 10 mm Countersink, Non-Sterile | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
48 | 00850017962125 | 10-2009-P | 10-2009-P | 9 mm x 7.5 mm Cannulated Drill and 9 mm Countersink, Non-Sterile | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
49 | 00850017962118 | 10-2008-P | 10-2008-P | 8 mm x 7 mm Cannulated Drill and 8 mm Countersink, Non-Sterile | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |
50 | 00850017962101 | 10-2007-P | 10-2007-P | 7 mm x 6.5 mm Cannulated Drill and 7 mm Countersink, Non-Sterile | S-Core™ | SUBCHONDRAL SOLUTIONS, INC. |