Other products from "SIGNATURE ORTHOPAEDICS PTY LTD"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 09348215057299 112-152-243 LXH Orthopedic Manual Surgical Instrument 1 Acetabular Reamer 43mm
2 09348215038892 112-152-198 HWT Template 1 Trial Cups
3 09348215062200 111-40-1413 MEH,LPH,KWZ Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calc Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate,Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented,Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer 2 World Hip Stem Size 4S
4 09348215046385 122-16-0338 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Sizer Tower
5 09348215061777 192-072-066 HTW Bit, Drill 1 Optimus Drill Q – 4.5mm 20mm
6 09348215061982 192-11-1232 The saleable unit (device count) is 1, there are 5 surgibit drills in the saleable unit HTW Bit, Drill 1 3.2 x 230 mm Surgibit Drill
7 09348215061944 192-162-020 HTW Bit, Drill 1 Straight Trocar Pin with Shoulder 3.2x70
8 09348215061883 192-162-014 HTW Bit, Drill 1 Threaded Prill 3.2 x 90 mm
9 09348215061746 192-072-040 HTW Bit, Drill 1 Magnus Q
10 09348215061685 192-072-029 HTW Bit, Drill 1 Optimus Drill Q - 3.5mm 60mm
11 09348215058319 192-20-0105 KCT Sterilization Wrap Containers, Trays, Cassettes & Other Accessories 2 Blank Tray
12 09348215058135 132-14-0070 LXH Orthopedic Manual Surgical Instrument 1 T-Handle for Cork Screw
13 09348215058081 112-25-1666 LXH Orthopedic Manual Surgical Instrument 1 Screw Forceps
14 09348215057930 112-25-0096 LXH Orthopedic Manual Surgical Instrument 1 Offset Final Implant Impacter
15 09348215057879 112-25-0065 LXH Orthopedic Manual Surgical Instrument 1 Infero-Posterior Acetabular Cabsule Retractor - Right
16 09348215057732 112-172-001 LXH Orthopedic Manual Surgical Instrument 1 Bent Cup Inserter
17 09348215057411 112-152-438 LXH Orthopedic Manual Surgical Instrument 1 Low Profile Acetabular Reamer 38
18 09348215057237 112-15-8656 HWT Template 1 Lateralised 10 Hood Trial Liner : SIZE 36/56-58mm
19 09348215057138 192-072-005 HTW Bit, Drill 1 Carrier Pin
20 09348215057084 122-15-0452 KCT Sterilization Wrap Containers, Trays, Cassettes & Other Accessories 2 Genius-A Instrument Case 3 Tibia+Trials
21 09348215056964 122-15-0084 MDM Instrument, Manual, Surgical, General Use 1 Tibial Offset Cutting Block : SIZE Left 7
22 09348215056919 122-102-292 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Genius Knee System Tibial Tray 2
23 09348215056896 122-102-260 MDM Instrument, Manual, Surgical, General Use 1 Femoral Notch Guide 6
24 09348215056698 122-102-217 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Tibial Trial Insert 4
25 09348215056681 122-102-216 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Tibial Trial Insert 3
26 09348215056544 122-102-157 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Tibial Trial Tray 2
27 09348215056414 122-102-133 LXH Orthopedic Manual Surgical Instrument 1 Femoral Notch Reamer 0
28 09348215056407 122-102-100 MDM Instrument, Manual, Surgical, General Use 1 Fixed Reference Femoral Sizer Stylus
29 09348215056230 111-201-612 HWT Template 1 Aria Stem Size 12 Template
30 09348215056193 111-201-608 HWT Template 1 Aria Stem Size 8 Template
31 09348215056186 111-201-607 HWT Template 1 Aria Stem Size 7 Template
32 09348215056117 111-201-600 HWT Template 1 Aria Stem Size 0 Template
33 09348215056100 112-34-1012 HWT Template 1 Remedy Stem Size 12 Template
34 09348215056070 112-34-1009 HWT Template 1 Remedy Stem Size 9 Template
35 09348215055981 112-34-1000 HWT Template 1 Remedy Stem Size 0 Template
36 09348215055936 112-212-164 HWT Template 1 Origin Stem Size 14 Template
37 09348215055844 112-212-026 LXH Orthopedic Manual Surgical Instrument 1 Stem Positioner Unibody
38 09348215055820 112-212-022 LXH Orthopedic Manual Surgical Instrument 1 Trochanteric Canal Reamer
39 09348215055790 111-182-024 LXH Orthopedic Manual Surgical Instrument 1 Origin DAA Trial Neck HO
40 09348215055738 111-18-1308 LXH Orthopedic Manual Surgical Instrument 1 Type A Broach Size 13
41 09348215055479 111-241-502 LXH Orthopedic Manual Surgical Instrument 1 Broach 50 size 2
42 09348215055363 111-241-351 LXH Orthopedic Manual Surgical Instrument 1 Broach 35.5 size 1
43 09348215055189 192-11-0225 The saleable unit (device count) is 1, there are 5 surgibit drills in the saleable unit HTW Bit, Drill 1 2.5 x 300 mm Surgibit Drill
44 09348215055141 192-11-0211 The saleable unit (device count) is 1, there are 5 surgibit drills in the saleable unit HTW Bit, Drill 1 1.1 x 300 mm Surgibit Drill
45 09348215055080 192-11-0132 The saleable unit (device count) is 1, there are 5 surgibit drills in the saleable unit HTW Bit, Drill 1 3.2 x 230 mm Surgibit Drill
46 09348215055059 192-11-0122 The saleable unit (device count) is 1, there are 5 surgibit drills in the saleable unit HTW Bit, Drill 1 2.1 x 200 mm Surgibit Drill
47 09348215055004 192-11-0111 The saleable unit (device count) is 1, there are 5 surgibit drills in the saleable unit HTW Bit, Drill 1 1.1 x 100 mm Surgibit Drill
48 09348215054885 192-11-0011 The saleable unit (device count) is 1, there are 5 surgibit drills in the saleable unit HTW Bit, Drill 1 1.1 x 100 mm Surgibit Drill
49 09348215053758 D111-16-0250 JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented 2 Cement Plug
50 09348215053741 D111-16-0185 JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented 2 Cement Plug
Other products with the same Product Code "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
9 10885862621931 SPI-046699 SPI-046699 Special Pinned Femoral RT- INT/ LT-EXT Rotation Adjustment Block Truliant EXACTECH, INC.
10 10885862621924 SPI-046300 SPI-046300 Special Pinned Femoral LT-INT / RT- EXT Rotation Adjustment Block Truliant EXACTECH, INC.
11 10885862621528 SPI-046441 SPI-046441 SPECIAL VAN DE LEUR TIBIAL RESECTOR, UPPER ASSEMBLY Truliant EXACTECH, INC.
12 10885862618719 SPI-046412 SPI-046412 SPECIAL LPI TIBIAL RESECETION BLOCK, RIGHT, WIDE SLOT Truliant EXACTECH, INC.
13 10885862618702 SPI-046411 SPI-046411 SPECIAL LPI TIBIAL RESECETION BLOCK, LEFT, WIDE SLOT Truliant EXACTECH, INC.
14 10885862618214 SPI-046319 SPI-046319 Truliant EXACTECH, INC.
15 10885862618207 SPI-046022 SPI-046022 SPECIAL VAN DE LEUR TIBIAL RESECTOR, SHAFT ASSEMBLY Truliant EXACTECH, INC.
16 10885862618146 SPI-046017 SPI-046017 SPECIAL VAN DE LEUR TIBIAL RESECTOR, ANKLE YOKE Truliant EXACTECH, INC.
17 10885862617989 SPI-038032-60 SPI-038032-60 Truliant EXACTECH, INC.
18 10885862617972 SPI-045747-35 SPI-045747-35 Truliant EXACTECH, INC.
19 10885862617965 SPI-045745-29 SPI-045745-29 Truliant EXACTECH, INC.
20 10885862617668 SPI-045404 SPI-045404 Truliant EXACTECH, INC.
21 10885862617453 SPI-044689 SPI-044689 Truliant EXACTECH, INC.
22 10885862617217 SPI-044794 SPI-044794 Truliant EXACTECH, INC.
23 10885862617132 SPI-044447 SPI-044447 Truliant EXACTECH, INC.
24 10885862610195 SPI-044406 SPI-044406 Truliant EXACTECH, INC.
25 10885862606884 SPI-041553-32 SPI-041553-32 Truliant EXACTECH, INC.
26 10885862606877 SPI-041550-5 SPI-041550-5 Truliant EXACTECH, INC.
27 10885862606860 SPI-041550-4 SPI-041550-4 Truliant EXACTECH, INC.
28 10885862606853 SPI-041550-3 SPI-041550-3 Truliant EXACTECH, INC.
29 10885862606846 SPI-041550-2 SPI-041550-2 Truliant EXACTECH, INC.
30 10885862606839 SPI-041550-1 SPI-041550-1 Truliant EXACTECH, INC.
31 10885862605672 SPI-040853 SPI-040853 Truliant EXACTECH, INC.
32 10885862605665 SPI-040844 SPI-040844 Truliant EXACTECH, INC.
33 10885862605542 SPI-040738 SPI-040738 Truliant EXACTECH, INC.
34 10885862603579 SPI-040344 SPI-040344 Truliant EXACTECH, INC.
35 10885862603562 SPI-040343 SPI-040343 Truliant EXACTECH, INC.
36 10885862603203 SPI-040152 SPI-040152 Truliant EXACTECH, INC.
37 10885862603128 SPI-039661-60 SPI-039661-60 Truliant EXACTECH, INC.
38 10885862603111 SPI-039661-50 SPI-039661-50 Truliant EXACTECH, INC.
39 10885862603104 SPI-039661-45 SPI-039661-45 Truliant EXACTECH, INC.
40 10885862603098 SPI-039661-40 SPI-039661-40 Truliant EXACTECH, INC.
41 10885862603081 SPI-039661-35 SPI-039661-35 Truliant EXACTECH, INC.
42 10885862603074 SPI-039661-30 SPI-039661-30 Truliant EXACTECH, INC.
43 10885862603067 SPI-039661-25 SPI-039661-25 Truliant EXACTECH, INC.
44 10885862603050 SPI-039661-20 SPI-039661-20 Truliant EXACTECH, INC.
45 10885862603043 SPI-039661-15 SPI-039661-15 Truliant EXACTECH, INC.
46 10885862603036 SPI-039661-10 SPI-039661-10 Truliant EXACTECH, INC.
47 10885862603029 SPI-039661-00 SPI-039661-00 Truliant EXACTECH, INC.
48 10885862603012 SPI-039670-R SPI-039670-R Truliant EXACTECH, INC.
49 10885862603005 SPI-039670-L SPI-039670-L Truliant EXACTECH, INC.
50 10885862602589 SPI-039616 SPI-039616 Truliant EXACTECH, INC.