Other products from "DEPUY (IRELAND)"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 10603295261148 L93502 L93502 REEF LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 REEF
2 10603295261131 L93501 L93501 REEF LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 REEF
3 10603295547532 6505-36-008 650536008 INHANCE SHOULDER SYSTEM GLENOSPHERE TRIAL Ø36 +8mm HWT TEMPLATE 1 INHANCE
4 10603295539414 6205-10-104 620510104 INHANCE SHOULDER SYSTEM CONVEX IMPACTOR TIP HWA IMPACTOR 1 INHANCE
5 10603295525257 122128055 122128055 BI-MENTUM ALTRX LINER 55/28 LZO,MEH Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented,Prosthesis, hip, semi-constrained, uncemented, metal / polymer, non-porous, calcium phosphate 2 BI-MENTUM ALTRX
6 10603295515708 4831-36-015 483136015 TRIAL HEAD 36mm +1.5 HWT TEMPLATE 1 NA
7 10603295530725 2317-70-423 231770423 DELTA XTEND Peripheral locking screwdriver end cap with spring HXX SCREWDRIVER 1 DELTA XTEND
8 10603295524120 4800-00-210 480000210 EMPHASYS ACETABULAR ALUMINUM CADDY ANCILLARY FSM TRAY, SURGICAL, INSTRUMENT 1 EMPHASYS
9 10603295261629 L95092 L95092 KAR LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 KAR
10 10603295324508 L46818 L46818 Gyros Base Box 2 FSM TRAY, SURGICAL, INSTRUMENT 1 GYROS
11 10603295493549 2544-11-003 254411003 ATTUNE KNEE SYSTEM ATTUNE SYSTEM IMPACTOR HWA IMPACTOR 1 ATTUNE
12 10603295423324 2544-01-017 254401017 ATTUNE IMPACTION HANDLE HWA IMPACTOR 1 ATTUNE
13 10603295324539 L46844 L46844 GYROS LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 GYROS
14 10603295440574 2506-30-102 250630102 ATTUNE KNEE SYSTEM REVISION OFFSET DRILL HTW BIT, DRILL 1 ATTUNE
15 10603295434351 9505-05-171 950505171 Reach KNEE CASE 3 FSM TRAY, SURGICAL, INSTRUMENT 1 NA
16 10603295261346 L93554 L93554 REEF LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 REEF
17 10603295261704 L95122 L95122 PANIER 2 KAR FSM TRAY, SURGICAL, INSTRUMENT 1 NA
18 10603295423560 2545-01-706 254501706 ATTUNE PS TRIALS SIZE 6-8 FSM TRAY, SURGICAL, INSTRUMENT 1 ATTUNE
19 10603295261674 L95119 L95119 PLATEAU SYNOPTIQUE 1 KAR FSM TRAY, SURGICAL, INSTRUMENT 1 NA
20 10603295261667 L95099 L95099 KAR LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 KAR
21 10603295381105 1140-10-044 114010044 GLOBAL ICON Stemless Shoulder System Anchor Plate Size 44 HA PKC Prosthesis, total anatomic shoulder, uncemented metaphyseal humeral stem with no Prosthesis, total anatomic shoulder, uncemented metaphyseal humeral stem with no diaphyseal incursion, semi-constrained 2 GLOBAL ICON
22 10603295285953 2407-42-209 240742209 DELTA CTA REV TRIAL CUP EPI36 D42 +9mm HWT TEMPLATE 1 DELTA CTA
23 10603295260295 L85878 L85878 TRAY 1 - INSERT 1 FSM TRAY, SURGICAL, INSTRUMENT 1 NA
24 10603295243182 9625-75-000 962575000 ELITE FEMORAL HEAD +0 9/10 TAPER Diameter 32mm JDI Prosthesis, hip, semi-constrained, metal/polymer, cemented 2 ELITE
25 10603295089612 2128-61-050 212861050 GLOBAL ADVANTAGE GLENOID CASE & INSERTS FSM TRAY, SURGICAL, INSTRUMENT 1 GLOBAL ADVANTAGE
26 10603295085508 2100-22-000 210022000 GLOBAL UNITE X-RAY TEMPLATES HWT TEMPLATE 1 GLOBAL UNITE
27 10603295077060 1976-17-190 197617190 RECLAIM REVISION HIP SYSTEM DISTAL TAPERED STEM 17mm X 190mm STRAIGHT LZO,KWA Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented,Prosthesis, hip, semi-constrained (metal uncemented acetabular component) 2 RECLAIM
28 10603295043553 1513-12-110 151312110 ATTUNE KNEE SYSTEM REVISION PRESSFIT STEM 12X110MM MBH,JWH,NJL PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, CO PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing 2 ATTUNE
29 10603295261087 L93384 L93384 TRAY No.1 FSM TRAY, SURGICAL, INSTRUMENT 1 NA
30 10603295261070 L93383 L93383 TRAY COVER No.3 FSM TRAY, SURGICAL, INSTRUMENT 1 NA
31 10603295261063 L93382 L93382 TRAY COVER No.2 FSM TRAY, SURGICAL, INSTRUMENT 1 NA
32 10603295261056 L93381 L93381 TRAY COVER No. 1 FSM TRAY, SURGICAL, INSTRUMENT 1 NA
33 10603295261124 L93388 L93388 BOTTOM TRAY No. 3 FSM TRAY, SURGICAL, INSTRUMENT 1 NA
34 10603295261117 L93387 L93387 TOP TRAY , 3 FSM TRAY, SURGICAL, INSTRUMENT 1 NA
35 10603295261100 L93386 L93386 BOTTOM TRAY No.2 FSM TRAY, SURGICAL, INSTRUMENT 1 NA
36 10603295261094 L93385 L93385 TOP TRAY No.2 FSM TRAY, SURGICAL, INSTRUMENT 1 NA
37 10603295261179 L93512 L93512 REEF LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 REEF
38 10603295261162 L93505 L93505 REEF LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 REEF
39 10603295261155 L93503 L93503 REEF LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 REEF
40 10603295548683 3010-01-090 301001090 ACTIS HIP SYSTEM BROACH SIZE 9 QBO Instruments designed for press-fit osteochondral implants 2 ACTIS
41 10603295548676 3010-01-080 301001080 ACTIS HIP SYSTEM BROACH SIZE 8 QBO Instruments designed for press-fit osteochondral implants 2 ACTIS
42 10603295548669 3010-01-070 301001070 ACTIS HIP SYSTEM BROACH SIZE 7 QBO Instruments designed for press-fit osteochondral implants 2 ACTIS
43 10603295548652 3010-01-060 301001060 ACTIS HIP SYSTEM BROACH SIZE 6 QBO Instruments designed for press-fit osteochondral implants 2 ACTIS
44 10603295548645 3010-01-050 301001050 ACTIS HIP SYSTEM BROACH SIZE 5 QBO Instruments designed for press-fit osteochondral implants 2 ACTIS
45 10603295548638 3010-01-040 301001040 ACTIS HIP SYSTEM BROACH SIZE 4 QBO Instruments designed for press-fit osteochondral implants 2 ACTIS
46 10603295548621 3010-01-030 301001030 ACTIS HIP SYSTEM BROACH SIZE 3 QBO Instruments designed for press-fit osteochondral implants 2 ACTIS
47 10603295548614 3010-01-020 301001020 ACTIS HIP SYSTEM BROACH SIZE 2 QBO Instruments designed for press-fit osteochondral implants 2 ACTIS
48 10603295548607 3010-01-120 301001120 ACTIS HIP SYSTEM BROACH SIZE 12 QBO Instruments designed for press-fit osteochondral implants 2 ACTIS
49 10603295548591 3010-01-110 301001110 ACTIS HIP SYSTEM BROACH SIZE 11 QBO Instruments designed for press-fit osteochondral implants 2 ACTIS
50 10603295548584 3010-01-100 301001100 ACTIS HIP SYSTEM BROACH SIZE 10 QBO Instruments designed for press-fit osteochondral implants 2 ACTIS
Other products with the same Product Codes "JWH, MBH, OIY"
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 TKRR0000LLBL5 UKI0101-R UNIKO PointCloud™ Knee Instrument Kit Right PointCloud UNIK ORTHOPEDICS INC.
10 TKRR0000LID65 UKI0101-R UNIKO PointCloud™ Knee Instrument Kit Right PointCloud UNIK ORTHOPEDICS INC.
11 TKRR0000LI745 UKI0101-R UNIKO PointCloud™ Knee Instrument Kit Right PointCloud UNIK ORTHOPEDICS INC.
12 TKRR0000LI105 UKI0101-R UNIKO PointCloud™ Knee Instrument Kit Right PointCloud UNIK ORTHOPEDICS INC.
13 TKRR0000LD2D5 UKI0101-R UNIKO PointCloud™ Knee Instrument Kit Right PointCloud UNIK ORTHOPEDICS INC.
14 TKRR0000LB3B5 UKI0101-R UNIKO PointCloud™ Knee Instrument Kit Right PointCloud UNIK ORTHOPEDICS INC.
15 TKRR0000L6855 UKI0101-R UNIKO PointCloud™ Knee Instrument Kit Right PointCloud UNIK ORTHOPEDICS INC.
16 TKRR0000L6265 UKI0101-R UNIKO PointCloud™ Knee Instrument Kit Right PointCloud UNIK ORTHOPEDICS INC.
17 TKRR0000L5K05 UKI0101-R UNIKO PointCloud™ Knee Instrument Kit Right PointCloud UNIK ORTHOPEDICS INC.
18 TKRR0000L4F85 UKI0101-R UNIKO PointCloud™ Knee Instrument Kit Right PointCloud UNIK ORTHOPEDICS INC.
19 TKRR0000FK065 UKI0101-R UNIKO PointCloud™ Knee Instrument Kit Right PointCloud UNIK ORTHOPEDICS INC.
20 TKRR0000FI7I5 UKI0101-R UNIKO PointCloud™ Knee Instrument Kit Right PointCloud UNIK ORTHOPEDICS INC.
21 TKRR0000FF8D5 UKI0101-R UNIKO PointCloud™ Knee Instrument Kit Right PointCloud UNIK ORTHOPEDICS INC.
22 TKRR0000FF295 UKI0101-R UNIKO PointCloud™ Knee Instrument Kit Right PointCloud UNIK ORTHOPEDICS INC.
23 TKRR0000FB3F5 UKI0101-R UNIKO PointCloud™ Knee Instrument Kit Right PointCloud UNIK ORTHOPEDICS INC.
24 TKRR0000F4995 UKI0101-R UNIKO PointCloud™ Knee Instrument Kit Right PointCloud UNIK ORTHOPEDICS INC.
25 TKRR0000F17L5 UKI0101-R UNIKO PointCloud™ Knee Instrument Kit Right PointCloud UNIK ORTHOPEDICS INC.
26 TKRR0000DFL65 UKI0101-R UNIKO PointCloud™ Knee Instrument Kit Right PointCloud UNIK ORTHOPEDICS INC.
27 TKRR0000DF825 UKI0101-R UNIKO PointCloud™ Knee Instrument Kit Right PointCloud UNIK ORTHOPEDICS INC.
28 TKRL0000LL595 UKI0101-L UNIKO PointCloud™ Knee Instrument Kit Left PointCloud UNIK ORTHOPEDICS INC.
29 TKRL0000LK015 UKI0101-L UNIKO PointCloud™ Knee Instrument Kit Left PointCloud UNIK ORTHOPEDICS INC.
30 TKRL0000LF225 UKI0101-L UNIKO PointCloud™ Knee Instrument Kit Left PointCloud UNIK ORTHOPEDICS INC.
31 TKRL0000LDF45 UKI0101-L UNIKO PointCloud™ Knee Instrument Kit Left PointCloud UNIK ORTHOPEDICS INC.
32 TKRL0000LBI35 UKI0101-L UNIKO PointCloud™ Knee Instrument Kit Left PointCloud UNIK ORTHOPEDICS INC.
33 TKRL0000L6F15 UKI0101-L UNIKO PointCloud™ Knee Instrument Kit Left PointCloud UNIK ORTHOPEDICS INC.
34 TKRL0000L55K5 UKI0101-L UNIKO PointCloud™ Knee Instrument Kit Left PointCloud UNIK ORTHOPEDICS INC.
35 TKRL0000L3D05 UKI0101-L UNIKO PointCloud™ Knee Instrument Kit Left PointCloud UNIK ORTHOPEDICS INC.
36 TKRL0000FLK35 UKI0101-L UNIKO PointCloud™ Knee Instrument Kit Left PointCloud UNIK ORTHOPEDICS INC.
37 TKRL0000FKD15 UKI0101-L UNIKO PointCloud™ Knee Instrument Kit Left PointCloud UNIK ORTHOPEDICS INC.
38 TKRL0000FK6D5 UKI0101-L UNIKO PointCloud™ Knee Instrument Kit Left PointCloud UNIK ORTHOPEDICS INC.
39 TKRL0000FID95 UKI0101-L UNIKO PointCloud™ Knee Instrument Kit Left PointCloud UNIK ORTHOPEDICS INC.
40 TKRL0000FI105 UKI0101-L UNIKO PointCloud™ Knee Instrument Kit Left PointCloud UNIK ORTHOPEDICS INC.
41 TKRL0000FFLL5 UKI0101-L UNIKO PointCloud™ Knee Instrument Kit Left PointCloud UNIK ORTHOPEDICS INC.
42 TKRL0000FDFI5 UKI0101-L UNIKO PointCloud™ Knee Instrument Kit Left PointCloud UNIK ORTHOPEDICS INC.
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45 TKRL0000F8845 UKI0101-L UNIKO PointCloud™ Knee Instrument Kit Left PointCloud UNIK ORTHOPEDICS INC.
46 TKRL0000F5635 UKI0101-L UNIKO PointCloud™ Knee Instrument Kit Left PointCloud UNIK ORTHOPEDICS INC.
47 TKRL0000F30I5 UKI0101-L UNIKO PointCloud™ Knee Instrument Kit Left PointCloud UNIK ORTHOPEDICS INC.
48 TKRL0000F1L25 UKI0101-L UNIKO PointCloud™ Knee Instrument Kit Left PointCloud UNIK ORTHOPEDICS INC.
49 10885862621931 SPI-046699 SPI-046699 Special Pinned Femoral RT- INT/ LT-EXT Rotation Adjustment Block Truliant EXACTECH, INC.
50 10885862621924 SPI-046300 SPI-046300 Special Pinned Femoral LT-INT / RT- EXT Rotation Adjustment Block Truliant EXACTECH, INC.