No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 00885556051375 | 71930717 | 71930717 | SYNERGY PC FEM SZ18 130MM | LPH | PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED | 2 | SYNERGY |
2 | 00885556799789 | 71075113B | 71075113B | SMART TSF FULL RING 130MM BLUE | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | SMART TSF |
3 | 00885556765357 | E0016663-6 | E0016663-6 | HANDLE | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | Legion |
4 | 00885556076538 | 913374 | 913374 | STAPLE 1.16X3.8X3.4 | JDR | STAPLE, FIXATION, BONE | 2 | NA |
5 | 00885556885208 | E0017815-2 | E0017815-2 | SHORTENED 180 2/3 RING | JDW | PIN, FIXATION, THREADED | 2 | Ex-Fix |
6 | 00885556883051 | E0017793-1 | E0017793-1 | MODIFIED META NAIL DROP | HSB | ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES | 2 | Meta Nail |
7 | 00885556867969 | E0017558-7 | E0017558-7 | FLEXIBLE I/M ROD | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | Journey II |
8 | 00885556816721 | E0017448-3 | E0017448-3 | MODIFIED HEX DRIVER | HWR | DRIVER, PROSTHESIS | 1 | Polar |
9 | 00885556810484 | E0017443-1 | E0017443-1 | JII TIBIAL BLOCK - LEFT | FZX | Guide, surgical, instrument | 1 | JII |
10 | 00885556806326 | E0017367-11 | E0017367-11 | MODIFIED R3 INSERTER | JDI | Prosthesis, hip, semi-constrained, metal/polymer, cemented | 2 | R3 |
11 | 00885556805770 | E0017337-1 | E0017337-1 | JII FLEXION SPACER BLOCK | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | JII |
12 | 00885556804827 | E0017314-9 | E0017314-9 | AP BLOCK SZ 8 | FZX | Guide, surgical, instrument | 1 | Legion |
13 | 00885556802410 | E0017267-1 | E0017267-1 | TIBIAL STEM TRIAL - 10MM X 70MM | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | Legion |
14 | 00885556801673 | E0017241-1 | E0017241-1 | MIS DA X-BAR | JDG | Prosthesis, hip, femoral component, cemented, metal | 2 | R3 |
15 | 00885556800812 | E0017230-1 | E0017230-1 | 2MM RECUT BLOCK | HWT | TEMPLATE | 1 | Journey II |
16 | 00885556795255 | E0017150-1 | E0017150-1 | 11MM DEEP FLUTED END CUTTING REAMER | HTO | REAMER | 1 | Trigen |
17 | 00885556793893 | E0017119-7 | E0017119-7 | MIS ACETABULAR REAMER 58MM | HTO | REAMER | 1 | R3 |
18 | 00885556791905 | E0017091-2 | E0017091-2 | TIBIAL CUTTING BLOCK - RT | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | Legion |
19 | 00885556790229 | E0017054-1 | E0017054-1 | MODULAR FIN PUNCH HANDLE | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | JII |
20 | 00885556783313 | E0016980-3 | E0016980-3 | UPPER TIBIAL GUIDE | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | Journey II |
21 | 00885556777954 | E0016892-1 | E0016892-1 | 9MM REAMER HEAD | HTO | REAMER | 1 | Trigen |
22 | 00885556775103 | E0016853-3 | E0016853-3 | EXTENDED T8 DRIVER SHAFT | HXX | SCREWDRIVER | 1 | PERI-LOC |
23 | 00885556773673 | ROB20000 | ROB20000 | CORI ROBOTICS USA | OLO | Orthopedic stereotaxic instrument | 2 | Real Intelligence |
24 | 00885556771013 | E0016765-1 | E0016765-1 | MODIFIED ANGEL WING | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | Legion |
25 | 00885556770566 | E0016753-1 | E0016753-1 | FLUTED CURVED CANNULATED AWL | HWJ | AWL | 1 | Trigen |
26 | 00885556763742 | 71170734 | 71170734 | EVOS LARGE PROXIMAL HUMERUS PLATE TRAY | FSM | TRAY, SURGICAL, INSTRUMENT | 1 | EVOS |
27 | 00885556763155 | E0016528-7 | E0016528-7 | SZ 51MM BRIDGEBACK REAMER | HTO | REAMER | 1 | R3 |
28 | 00885556762189 | 72581004 | 72581004 | EVOS 3.5MM/4.5MM UTILITY PLATE 4H 147MM | HRS | Plate, fixation, bone | 2 | EVOS |
29 | 00885556757192 | E0016586-2 | E0016586-2 | 8.5MM REAMER HEAD | HWE | INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT | 1 | Trigen |
30 | 00885556757116 | E0016583-1 | E0016583-1 | RAT TAIL RASP | JDG | Prosthesis, hip, femoral component, cemented, metal | 2 | Polar |
31 | 00885556755068 | ROB10000 | ROB10000 | CORI Starter Kit | OLO | Orthopedic stereotaxic instrument | 2 | CORI |
32 | 00885556753682 | E0016536-2 | E0016536-2 | ZUK SPACER BLOCK - 11MM | HWT | TEMPLATE | 1 | Uni |
33 | 00885556752081 | 72546585N | 72546585N | EVOS 6.5MM X 85MM CANNULATED SCREW | HWC | Screw, fixation, bone | 2 | EVOS |
34 | 00885556740422 | E0016327-2 | E0016327-2 | IM ROD SHORT | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | JII |
35 | 00885556737392 | E0016303-3 | E0016303-3 | OFFSET FIXATION ROD | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | JII |
36 | 00885556733837 | E0016253-2 | E0016253-2 | LARGE BLADE | GAD | RETRACTOR | 1 | Anthology |
37 | 00885556725337 | E0016116-2 | E0016116-2 | 2MM RECUT BLOCK | HWT | TEMPLATE | 1 | Legion |
38 | 00885556722701 | 21-8020 | 21-8020 | DEPTH GAGE | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A |
39 | 00885556627020 | PFSI00040 | PFSI00040 | Stride Poly Insert Size D 9mm | HSX | PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | STRIDE |
40 | 00885556716274 | E0015966-1 | E0015966-1 | FEMORAL STYLUS | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | Legion |
41 | 00885556715536 | E0015722-1 | E0015722-1 | FEMORAL TRIAL PADDLE | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | Legion |
42 | 00885556626979 | PFSI00033 | PFSI00033 | Stride Poly Insert Size C 8mm | HSX | PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | STRIDE |
43 | 00885556713662 | 72411812 | 72411812 | EVOS 1.8MM X 12MM LOCKING PEG T7 | HRS | Plate, fixation, bone | 2 | EVOS |
44 | 00885556710357 | E0015809-1 | E0015809-1 | SIDE FEMORAL HEAD IMPACTOR | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | R3 |
45 | 00885556710418 | E0015860-1 | E0015860-1 | IM ALIGNMENT GUIDE WITH THUMB SCREWS | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | Legion |
46 | 00885556710241 | E0015781-3 | E0015781-3 | SPIKED ELEVATOR - STRAIGHT | HTE | ELEVATOR | 1 | Peri-loc |
47 | 00885556708675 | E0015708-5 | E0015708-5 | GII PS TRIAL INSERT 5-6 9MM | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | Legion |
48 | 00885556706978 | E0015771-1 | E0015771-1 | 2MM RECUT BLOCK | HWT | TEMPLATE | 1 | Legion |
49 | 00885556704561 | E0015694-2 | E0015694-2 | PATELLA DEPTH GAUGE - 5MM | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | Legion |
50 | 00885556704455 | E0015672-1 | E0015672-1 | JOURNEY CR FEMORAL IMPACTOR | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | Journey II |
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. |