Other products from "MODAL MANUFACTURING LLC"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 B035M341100601 M-3411-0060 Patella Trial 29mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
2 B035M340100901 M-3401-0090 Patella 38mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
3 B035M340100801 M-3401-0080 Patella 35mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
4 B035M340100701 M-3401-0070 Patella 32mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
5 B035M340100601 M-3401-0060 Patella 29mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
6 B035M331140251 M-3311-4025 UC CR Tibial Trial Insert Size 5 - 11mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
7 B035M331140241 M-3311-4024 UC CR Tibial Trial Insert Size 4 - 11mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
8 B035M342050051 M-3420-5005 Patellar Drill Guide 32mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
9 B035M342050411 Rev A M-3420-5041 Patellar Drill Guide 41mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
10 B035M342050071 M-3420-5007 Patellar Drill Guide 38mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
11 B035M342050061 M-3420-5006 Patellar Drill Guide 35mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
12 B035M342050041 M-3420-5004 Patellar Drill JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
13 B035M342050031 M-3420-5003 Patellar Cement Clamp JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
14 B035M342050021 M-3420-5002 Patellar Drill Guide 29mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
15 B035M342050011 M-3420-5001 Patellar Drill & Cement Clamp JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
16 B035M342050001 M-3420-5000 Patellar Resection Clamp JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
17 B035M341101001 Rev D M-3411-0100 XXL Patellar Trial 41mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
18 B035M341100901 M-3411-0090 Patella Trial 38mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
19 B035M341100801 M-3411-0080 Patella Trial 35mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
20 B035M341100701 M-3411-0070 Patella Trial 32mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
21 B035M332050540 Rev A M-3320-5054 Modular Tibia Insert Impactor JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
22 B035M332050001 M-3320-5000 Tibial Insert Impactor JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
23 B035M331140561 M-3311-4056 UC CR Tibial Trial Insert Size 6 - 18mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
24 B035M331140551 M-3311-4055 UC CR Tibial Trial Insert Size 5 - 18mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
25 B035M331140541 M-3311-4054 UC CR Tibial Trial Insert Size 4 - 18mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
26 B035M331140531 M-3311-4053 UC CR Tibial Trial Insert Size 3 - 18mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
27 B035M331140521 M-3311-4052 UC CR Tibial Trial Insert Size 2 - 18mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
28 B035M331140511 M-3311-4051 UC CR Tibial Trial Insert Size 1 - 18mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
29 B035M331140461 M-3311-4046 UC CR Tibial Trial Insert Size 6 - 15mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
30 B035M331140451 M-3311-4045 UC CR Tibial Trial Insert Size 5 - 15mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
31 B035M331140441 M-3311-4044 UC CR Tibial Trial Insert Size 4 - 15mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
32 B035M331140431 M-3311-4043 UC CR Tibial Trial Insert Size 3 - 15mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
33 B035M331140421 M-3311-4042 UC CR Tibial Trial Insert Size 2 - 15mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
34 B035M331140411 M-3311-4041 UC CR Tibial Trial Insert Size 1 - 15mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
35 B035M331140361 M-3311-4036 UC CR Tibial Trial Insert Size 6 - 13mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
36 B035M331140351 M-3311-4035 UC CR Tibial Trial Insert Size 5 - 13mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
37 B035M331140341 M-3311-4034 UC CR Tibial Trial Insert Size 4 - 13mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
38 B035M331140331 M-3311-4033 UC CR Tibial Trial Insert Size 3 - 13mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
39 B035M331140321 M-3311-4032 UC CR Tibial Trial Insert Size 2 - 13mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
40 B035M331140311 M-3311-4031 UC CR Tibial Trial Insert Size 1 - 13mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
41 B035M331140261 M-3311-4026 UC CR Tibial Trial Insert Size 6 - 11mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
42 B035M331140231 M-3311-4023 UC CR Tibial Trial Insert Size 3 - 11mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
43 B035M331140221 M-3311-4022 UC CR Tibial Trial Insert Size 2 - 11mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
44 B035M331140211 M-3311-4021 UC CR Tibial Trial Insert Size 1 - 11mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
45 B035M331140161 M-3311-4016 UC CR Tibial Trial Insert Size 6 - 9mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
46 B035M331140151 M-3311-4015 UC CR Tibial Trial Insert Size 5 - 9mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
47 B035M331140141 M-3311-4014 UC CR Tibial Trial Insert Size 4 - 9mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
48 B035M322050021 M-3220-5002 Tibial EM Guide JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
49 B035M331140131 M-3311-4013 UC CR Tibial Trial Insert Size 3 - 9mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
50 B035M331140121 M-3311-4012 UC CR Tibial Trial Insert Size 2 - 9mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Modal Total Knee System
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.