Other products from "GLOBUS MEDICAL, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00849044083866 652.632 Single Trial, 32mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
2 00849044083859 652.630 Single Trial, 30mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
3 00849044092882 688.400 Rod Cutter LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
4 00849044076011 601.405 Trial, Parallel, 5mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
5 00849044072389 685.420 Calipers LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
6 00849044056075 624.613 REVERE Power Bender LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
7 00849044092875 688.368 Small Plate Caddy LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
8 00849044092868 688.367 AP Inserter Caddy LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
9 00849044092851 688.366 AP Inserter, 44-55mm Plate LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
10 00849044092844 688.365 AP Inserter, 35-41mm Plate LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
11 00849044092905 688.460 SP-Fix ARC Plate Pincher LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
12 00849044092899 688.450 Plate Pincher LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
13 00849044086089 671.303 Screwdriver Sleeve LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
14 00849044092837 688.351 Lateral Barrel Inserter, 44-55mm Plate LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
15 00849044092820 688.350 Lateral Barrel Inserter, 35-41mm Plate LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
16 00849044092813 688.331 Removal Driver LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
17 00849044092806 688.330 Hex Key LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
18 00849044092790 688.320 Implant Compressor LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
19 00849044092783 688.315 Rod Holder LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
20 00849044092776 688.314 Barrel Holder LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
21 00849044092769 688.311 Plate Holder, 44-55mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
22 00849044092752 688.310 Plate Holder, 35-41mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
23 00849044092745 688.300 Distractor LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
24 00849044092738 688.275 Rod Trial LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
25 00849044092721 688.255 Plate Trial, 55mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
26 00849044092714 688.250 Plate Trial, 50mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
27 00849044092707 688.247 Plate Trial, 47mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
28 00849044092691 688.244 Plate Trial, 44mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
29 00849044092684 688.241 Plate Trial, 41mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
30 00849044092677 688.238 Plate Trial, 38mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
31 00849044092660 688.235 Plate Trial, 35mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
32 00849044092653 688.232 Plate Trial, 32mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
33 00849044092646 688.229 Plate Trial, 29mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
34 00849044092615 688.170 LP-Ti Barrel Trial, 20mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
35 00849044092608 688.168 LP-Ti Barrel Trial, 18mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
36 00849044092592 688.166 LP-Ti Barrel Trial, 16mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
37 00849044092585 688.164 LP-Ti Barrel Trial, 14mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
38 00849044092578 688.162 LP-Ti Barrel Trial, 12mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
39 00849044092561 688.160 LP-Ti Barrel Trial, 10mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
40 00849044092554 688.158 LP-Ti Barrel Trial, 8mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
41 00849044092530 688.120 Trial, 20mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
42 00849044092523 688.118 Trial, 18mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
43 00849044092516 688.116 Trial, 16mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
44 00849044092509 688.114 Trial, 14mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
45 00849044092493 688.112 Trial, 12mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
46 00849044092486 688.110 Trial, 10mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
47 00849044092479 688.108 Trial, 8mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
48 00849044092462 688.075 Rasp LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
49 00849044092455 688.060 Spinous Process Rake LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
50 00849044089837 524.885 8.5mm REVERE Monoaxial Reduction Screw, 90mm KWP,MNH,KWQ,NKB,MNI APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spondylolisthesis spinal fixa APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spondylolisthesis spinal fixation,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,Orthosis, spinal pedicle fixation, for degenerative disc disease,ORTHOSIS, SPINAL PEDICLE FIXATION 2 REVERE
Other products with the same Product Codes "OIY, JWH"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 28031497001900 SPK0722 Temporary Augmented Tibial Stem Spacer with gentamicin. Interspace Knee ATS is c Temporary Augmented Tibial Stem Spacer with gentamicin. Interspace Knee ATS is composed of fully formed gentamicin/polymethylmethacrylate (PMMA), radio-opaque bone cement. The device is sterile and single-use.InterSpace Knee ATS is indicated for temporary use (maximum 180 days) as an adjunct to total knee replacement (TKR) in skeletally mature patients undergoing a two-stage procedure due to a septic process, and where a large tibial defect is present.InterSpace Knee ATS is applied on the tibial plate following removal of the existing implant and radical debridement. The device must be combined with the tibial component of InterSpace Knee. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection).InterSpace Knee ATS is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g. resection arthroplasty, fusion etc.). Because of the inherent mechanical limitations of the device material (gentamicin/ polymethylmethacrylate), the Interspace Knee ATS is only indicated for patients who will consistently use traditional mobility assist devices (e.g. crutches, walkers, canes) throughout the implantation period. Interspace Knee ATS 80/12 TECRES SPA
2 28031497001894 SPK0622 Temporary Augmented Tibial Stem Spacer with gentamicin. Interspace Knee ATS is c Temporary Augmented Tibial Stem Spacer with gentamicin. Interspace Knee ATS is composed of fully formed gentamicin/polymethylmethacrylate (PMMA), radio-opaque bone cement. The device is sterile and single-use.InterSpace Knee ATS is indicated for temporary use (maximum 180 days) as an adjunct to total knee replacement (TKR) in skeletally mature patients undergoing a two-stage procedure due to a septic process, and where a large tibial defect is present.InterSpace Knee ATS is applied on the tibial plate following removal of the existing implant and radical debridement. The device must be combined with the tibial component of InterSpace Knee. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection).InterSpace Knee ATS is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g. resection arthroplasty, fusion etc.). Because of the inherent mechanical limitations of the device material (gentamicin/ polymethylmethacrylate), the Interspace Knee ATS is only indicated for patients who will consistently use traditional mobility assist devices (e.g. crutches, walkers, canes) throughout the implantation period. Interspace Knee ATS 80/07 TECRES SPA
3 28031497001887 SPK0522 Temporary Augmented Tibial Stem Spacer with gentamicin. Interspace Knee ATS is c Temporary Augmented Tibial Stem Spacer with gentamicin. Interspace Knee ATS is composed of fully formed gentamicin/polymethylmethacrylate (PMMA), radio-opaque bone cement.The device is sterile and single-use.InterSpace Knee ATS is indicated for temporary use (maximum 180 days) as an adjunct to total knee replacement (TKR) in skeletally mature patients undergoing a two-stage procedure due to a septic process, and where a large tibial defect is present.InterSpace Knee ATS is applied on the tibial plate following removal of the existing implant and radical debridement. The device must be combined with the tibial component of InterSpace Knee. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection).InterSpace Knee ATS is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g. resection arthroplasty, fusion etc.). Because of the inherent mechanical limitations of the device material (gentamicin/ polymethylmethacrylate), the Interspace Knee ATS is only indicated for patients who will consistently use traditional mobility assist devices (e.g. crutches, walkers, canes) throughout the implantation period. Interspace Knee ATS 60/12 TECRES SPA
4 28031497001870 SPK0422 Temporary Augmented Tibial Stem Spacer with gentamicin. Interspace Knee ATS is c Temporary Augmented Tibial Stem Spacer with gentamicin. Interspace Knee ATS is composed of fully formed gentamicin/polymethylmethacrylate (PMMA), radio-opaque bone cement. The device is sterile and single-use.InterSpace Knee ATS is indicated for temporary use (maximum 180 days) as an adjunct to total knee replacement (TKR) in skeletally mature patients undergoing a two-stage procedure due to a septic process, and where a large tibial defect is present.InterSpace Knee ATS is applied on the tibial plate following removal of the existing implant and radical debridement. The device must be combined with the tibial component of InterSpace Knee. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection).InterSpace Knee ATS is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g. resection arthroplasty, fusion etc.). Because of the inherent mechanical limitations of the device material (gentamicin/ polymethylmethacrylate), the Interspace Knee ATS is only indicated for patients who will consistently use traditional mobility assist devices (e.g. crutches, walkers, canes) throughout the implantation period. Interspace Knee ATS 60/07 TECRES SPA
5 28031497001160 SPK0322 Temporary knee spacer with gentamicin. InterSpace Knee is composed of fully form Temporary knee spacer with gentamicin. InterSpace Knee is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement.The device is sterile and single-use.InterSpace Knee is indicated for temporary use (maximum 180 days) as a total knee replacement (TKR) in skeletally mature patients undergoing a two-stage procedure due to a septic process.InterSpace Knee is applied on the femoral condyles and on the tibial plate following removal of the existing implant and radical debridement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection).InterSpace Knee is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g. resection arthroplasty, fusion etc.). Because of the inherent mechanical limitations of the device material (gentamicin/polymethylmethacrylate), Interspace Knee is only indicated for patients who will consistently use traditional mobility assist devices (e.g. crutches, walkers, canes) throughout the implantation period. InterSpace Knee TECRES SPA
6 28031497000606 SPK0222 Temporary knee spacer with gentamicin. InterSpace Knee is composed of fully form Temporary knee spacer with gentamicin. InterSpace Knee is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement.The device is sterile and single-use.InterSpace Knee is indicated for temporary use (maximum of 180 days) as a total knee replacement (TKR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. InterSpace Knee is applied on the femoral condyles and on the tibial plate following removal of the existing implantand radical debridement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection). InterSpace Knee is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g., resection arthroplasty, fusion, etc.). InterSpace Knee TECRES SPA
7 28031497000590 SPK0122 Temporary knee spacer with gentamicin. InterSpace Knee is composed of fully form Temporary knee spacer with gentamicin. InterSpace Knee is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement.The device is sterile and single-use.InterSpace Knee is indicated for temporary use (maximum of 180 days) as a total knee replacement (TKR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. InterSpace Knee is applied on the femoral condyles and on the tibial plate following removal of the existing implantand radical debridement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection). InterSpace Knee is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g., resection arthroplasty, fusion, etc.). InterSpace Knee TECRES SPA
8 28031497000583 SPK0022 Temporary knee spacer with gentamicin. InterSpace Knee is composed of fully form Temporary knee spacer with gentamicin. InterSpace Knee is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement.The device is sterile and single-use.InterSpace Knee is indicated for temporary use (maximum of 180 days) as a total knee replacement (TKR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. InterSpace Knee is applied on the femoral condyles and on the tibial plate following removal of the existing implantand radical debridement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection). InterSpace Knee is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g., resection arthroplasty, fusion, etc.). InterSpace Knee TECRES SPA
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