Other products from "OSTEOMED LLC"
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
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34 10381780279471 2031004 2031004 K2™ Hemi Toe Implant System TOE PLATE K2™ Hemi Toe Implant System INTEGRA LIFESCIENCES CORPORATION
35 10381780257240 HEMISET K2™ Hemi Instrument Set (20-6000) K2™ ASCENSION ORTHOPEDICS, INC.
36 10381780237150 PIS89000 The Movement Great Toe proximal phalanx implant sizer allows for clear visualiza The Movement Great Toe proximal phalanx implant sizer allows for clear visualization of the implant size. Movement® ASCENSION ORTHOPEDICS, INC.
37 10381780237143 MIS89000 The Movement Great Toe metatarsal sizer allows for clear visualization of the im The Movement Great Toe metatarsal sizer allows for clear visualization of the implant size. Movement® ASCENSION ORTHOPEDICS, INC.
38 10381780236948 TRL89040PPH The Proximal Phalanx Hemi Trial is used to evaluate the size and fit of the implant. Movement® ASCENSION ORTHOPEDICS, INC.
39 10381780236931 TRL89040MT The Metatarsal Trial is used to evaluate the size and fit of the implant. Movement® ASCENSION ORTHOPEDICS, INC.
40 10381780236917 TRL89030PPH The Proximal Phalanx Hemi Trial is used to evaluate the size and fit of the implant. Movement® ASCENSION ORTHOPEDICS, INC.
41 10381780236900 TRL89030MT The Metatarsal Trial is used to evaluate the size and fit of the implant. Movement® ASCENSION ORTHOPEDICS, INC.
42 10381780236887 TRL89020PPH The Proximal Phalanx Hemi Trial is used to evaluate the size and fit of the implant. Movement® ASCENSION ORTHOPEDICS, INC.
43 10381780236870 TRL89020MT The Metatarsal Trial is used to evaluate the size and fit of the implant. Movement® ASCENSION ORTHOPEDICS, INC.
44 10381780236856 TRL89010PPH The Proximal Phalanx Hemi Trial is used to evaluate the size and fit of the implant. Movement® ASCENSION ORTHOPEDICS, INC.
45 10381780236849 TRL89010MT The Metatarsal Trial is used to evaluate the size and fit of the implant. Movement® ASCENSION ORTHOPEDICS, INC.
46 10381780234999 MOVEMNTINSTP The Movement Great Toe System is used for hemi- and total-arthroplasty procedure The Movement Great Toe System is used for hemi- and total-arthroplasty procedures. The hemi arthroplasty is intended for resurfacing of the 1st metatarsal head or the base of the proximal phalanx. The total arthroplasty is intended for resurfacing of the base of the 1st metatarso-phalangeal joint. This set includes metatarsal, proximal phalanx hemi, and proximal phalanx total trials to evaluate the size and fit of the appropriate implant. Instruments are also included to assist with the trials. Movement® ASCENSION ORTHOPEDICS, INC.
47 10381780116479 MGT89040PPH MGT89040PPH The Integra Movement Great Toe System phalangeal component is designed for resur The Integra Movement Great Toe System phalangeal component is designed for resurfacing the base of the proximal phalanx. The component is an anatomically designed, monolithic device. The device is made from cobalt chromium alloy with a commerically pure titanium plasma spray. The phalangeal component is intended as hemi-arthroplasty at the surface and is press-fit. Integra® MOVEMENT® Great Toe System ASCENSION ORTHOPEDICS, INC.
48 10381780116462 MGT89040MT MGT89040MT The Integra Movement Great Toe System metatarsal component is designed for resur The Integra Movement Great Toe System metatarsal component is designed for resurfacing the 1st metatarsal head. The component is an anatomically designed, monolithic device.The device is made from cobalt chromium alloy with a commercially pure titanium plasma spray. The metatarsal is intended as hemi-arthroplasty at the surface and is a press-fit. Integra® MOVEMENT® Great Toe System ASCENSION ORTHOPEDICS, INC.
49 10381780116455 MGT89030PPH MGT89030PPH The Integra Movement Great Toe System phalangeal component is designed for resur The Integra Movement Great Toe System phalangeal component is designed for resurfacing the base of the proximal phalanx. The component is an anatomically designed, monolithic device. The device is made from cobalt chromium alloy with a commerically pure titanium plasma spray. The phalangeal component is intended as hemi-arthroplasty at the surface and is press-fit. Integra® MOVEMENT® Great Toe System ASCENSION ORTHOPEDICS, INC.
50 10381780116448 MGT89030MT MGT89030MT The Integra Movement Great Toe System metatarsal component is designed for resur The Integra Movement Great Toe System metatarsal component is designed for resurfacing the 1st metatarsal head. The component is an anatomically designed, monolithic device.The device is made from cobalt chromium alloy with a commercially pure titanium plasma spray. The metatarsal is intended as hemi-arthroplasty at the surface and is a press-fit. Integra® MOVEMENT® Great Toe System ASCENSION ORTHOPEDICS, INC.