Other products from "ENCORE MEDICAL, L.P."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00190446735922 342-13-705 EMPOWR 3D KNEETM INS, 5R 13MM, VE OIY,JWH Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + add Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 DJO SURGICAL
2 00190446735915 341-13-705 EMPOWR 3D KNEETM INS, 5L 13MM, VE OIY,JWH Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + add Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 DJO SURGICAL
3 00190446735762 341-11-702 EMPOWR 3D KNEETM INS, 2L 11MM, VE OIY,JWH Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + add Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 DJO SURGICAL
4 00190446302636 414922 2.0 AND 2.7MM SCREW DRIVER HANDLE LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 DJO SURGICAL
5 00190446747482 800-05-096 DJO EMPOWR REVISION KNEE, FEMORAL TRIAL LOCATOR, SZ 6-11 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 DJO SURGICAL
6 00190446747468 800-05-095 DJO EMPOWR REVISION KNEE, FEMORAL TRIAL LOCATOR, SZ 2-5 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 DJO SURGICAL
7 00190446745266 800-05-094 DJO EMPOWR REVISION KNEE, FEMORAL FLEXION TOWER 0/3 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 DJO SURGICAL
8 00190446302605 414916 DISCOVERY XS HUM RES TEMPLATE HWT TEMPLATE 1 DJO SURGICAL
9 00190446736165 342-13-711 EMPOWR 3D KNEETM INS, 11R 13MM, VE JWH,OIY PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive 2 DJO SURGICAL
10 00190446302582 414913 DISCOVERY XS FOSSA REAMER HTO REAMER 1 DJO SURGICAL
11 00190446736158 341-13-711 EMPOWR 3D KNEETM INS, 11L 13MM, VE OIY,JWH Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + add Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 DJO SURGICAL
12 00190446302575 414912 DISCOVERY 5 STEP FOSSA REAMER HTO REAMER 1 DJO SURGICAL
13 00190446736141 342-11-711 EMPOWR 3D KNEETM INS, 11R 11MM, VE JWH,OIY PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive 2 DJO SURGICAL
14 00190446736134 341-11-711 EMPOWR 3D KNEETM INS, 11L 11MM, VE JWH,OIY PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive 2 DJO SURGICAL
15 00190446736127 342-13-710 EMPOWR 3D KNEETM INS, 10R 13MM, VE JWH,OIY PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive 2 DJO SURGICAL
16 00190446736110 341-13-710 EMPOWR 3D KNEETM INS, 10L 13MM, VE JWH,OIY PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive 2 DJO SURGICAL
17 00190446302292 414868 DISC 2.5MM RIGHT ULNA RASP HTQ BROACH 1 DJO SURGICAL
18 00190446736103 342-11-710 EMPOWR 3D KNEETM INS, 10R 11MM, VE JWH,OIY PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive 2 DJO SURGICAL
19 00190446302285 414867 DISC 2.5MM LEFT ULNA RASP HTQ BROACH 1 DJO SURGICAL
20 00190446736097 341-11-710 EMPOWR 3D KNEETM INS, 10L 11MM, VE OIY,JWH Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + add Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 DJO SURGICAL
21 00190446736080 342-13-709 EMPOWR 3D KNEETM INS, 9R 13MM, VE JWH,OIY PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive 2 DJO SURGICAL
22 00190446736073 341-13-709 EMPOWR 3D KNEETM INS, 9L 13MM, VE OIY,JWH Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + add Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 DJO SURGICAL
23 00190446736066 342-11-709 EMPOWR 3D KNEETM INS, 9R 11MM, VE OIY,JWH Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + add Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 DJO SURGICAL
24 00190446736059 341-11-709 EMPOWR 3D KNEETM INS, 9L 11MM, VE JWH,OIY PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive 2 DJO SURGICAL
25 00190446736042 342-13-708 EMPOWR 3D KNEETM INS, 8R 13MM, VE OIY,JWH Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + add Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 DJO SURGICAL
26 00190446736035 341-13-708 EMPOWR 3D KNEETM INS, 8L 13MM, VE JWH,OIY PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive 2 DJO SURGICAL
27 00190446736028 342-11-708 EMPOWR 3D KNEETM INS, 8R 11MM, VE OIY,JWH Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + add Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 DJO SURGICAL
28 00190446764335 803-03-241 MODULAR T-HANDLE, LINEAR PLUS LXH Orthopedic manual surgical instrument 1 DJO SURGICAL
29 00190446764274 800-99-161 EMPOWR REVISION KNEE, HALF-TRAY LID FSM TRAY, SURGICAL, INSTRUMENT 1 DJO SURGICAL
30 00190446757672 800-99-160 EMPOWR REVISION KNEE, OUTLIER TRAY, SZ: 2-3, 10-11 FSM TRAY, SURGICAL, INSTRUMENT 1 DJO SURGICAL
31 00190446301950 414820 DISC 3.5MM DIST HUMERAL RASP HTQ BROACH 1 DJO SURGICAL
32 00190446757665 800-99-159 EMPOWR REVISION KNEE, CORE TRAY, SZ: 4-9 FSM TRAY, SURGICAL, INSTRUMENT 1 DJO SURGICAL
33 00190446301912 414815 DISC 3.5X124MM PROX HUM RASP HTQ BROACH 1 DJO SURGICAL
34 00190446754282 800-05-098 DJO EMPOWR REVISION KNEE, STEM EXTENDER TRIAL, 15MM X 25MM JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 DJO SURGICAL
35 00190446753957 800-05-097 DJO EMPOWR REVISION KNEE, ANTERIOR CUT GUIDE, SIZE 6-11 FZX Guide, surgical, instrument 1 DJO SURGICAL
36 00190446750734 800-05-093 DJO EMPOWR REVISION KNEE, 3.5MM BALL END HEX DRIVER JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 DJO SURGICAL
37 00190446735663 800-05-122 DJO EMPOWR REVISION KNEE, DISTAL AUG TRIALS, SZ 10/11, 10MM JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 DJO SURGICAL
38 00190446735656 800-05-121 DJO EMPOWR REVISION KNEE, DISTAL AUG TRIALS, SZ 8/9, 10MM JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 DJO SURGICAL
39 00190446735649 800-05-120 DJO EMPOWR REVISION KNEE, DISTAL AUG TRIALS, SZ 6/7, 10MM JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 DJO SURGICAL
40 00190446301905 414814 DISC 3.5X84MM PROX HUM RASP HTQ BROACH 1 DJO SURGICAL
41 00190446735632 800-05-119 DJO EMPOWR REVISION KNEE, DISTAL AUG TRIALS, SZ 4/5, 10MM JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 DJO SURGICAL
42 00190446735625 800-05-118 DJO EMPOWR REVISION KNEE, DISTAL AUG TRIALS, SZ 2/3, 10MM JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 DJO SURGICAL
43 00190446735618 800-05-117 DJO EMPOWR REVISION KNEE, DISTAL AUG TRIALS, SZ 10/11, 5MM JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 DJO SURGICAL
44 00190446735601 800-05-116 DJO EMPOWR REVISION KNEE, DISTAL AUG TRIALS, SZ 8/9, 5MM JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 DJO SURGICAL
45 00190446296652 803-42-44K Trial Liner, EMPOWR Acetabular, 10°, 44K FZX Guide, surgical, instrument 1 DJO SURGICAL
46 00190446735595 800-05-115 DJO EMPOWR REVISION KNEE, DISTAL AUG TRIALS, SZ 6/7, 5MM JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 DJO SURGICAL
47 00190446735588 800-05-114 DJO EMPOWR REVISION KNEE, DISTAL AUG TRIALS, SZ 4/5, 5MM JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 DJO SURGICAL
48 00190446735571 800-05-113 DJO EMPOWR REVISION KNEE, DISTAL AUG TRIALS, SZ 2/3, 5MM JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 DJO SURGICAL
49 00190446735564 800-05-112 DJO EMPOWR REVISION KNEE, POST AUG TRIALS, SZ 10/11, 10MM JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 DJO SURGICAL
50 00190446735557 800-05-111 DJO EMPOWR REVISION KNEE, POST AUG TRIALS, SZ 8/9, 10MM JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 DJO SURGICAL
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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36 10885862603203 SPI-040152 SPI-040152 Truliant EXACTECH, INC.
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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.