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 | B278SB4044V03M0 | SB-4044V-03M | SB-4044V-03M | MODULAR REDUCED RESECTION COLLAR, 40MM X 44MM | ELEOS Limb Salvage System | ONKOS SURGICAL, INC. |
2 | B278SB3640V03M0 | SB-3640V-03M | SB-3640V-03M | MODULAR REDUCED RESECTION COLLAR, 36MM X 40MM | ELEOS Limb Salvage System | ONKOS SURGICAL, INC. |
3 | B278PB4000R03M0 | PB-4000R-03M | PB-4000R-03M | MODULAR POROUS BIOGRIP® COLLAR, 40MM, HA COATED | ELEOS Limb Salvage System With BioGrip | ONKOS SURGICAL, INC. |
4 | B278PB3600R03M0 | PB-3600R-03M | PB-3600R-03M | MODULAR POROUS BIOGRIP® COLLAR, 36MM, HA COATED | ELEOS Limb Salvage System With BioGrip | ONKOS SURGICAL, INC. |
5 | B278PB3200R03M0 | PB-3200R-03M | PB-3200R-03M | MODULAR POROUS BIOGRIP® COLLAR, 32MM, HA COATED | ELEOS Limb Salvage System With BioGrip | ONKOS SURGICAL, INC. |
6 | B278PB2800R03M0 | PB-2800R-03M | PB-2800R-03M | MODULAR POROUS BIOGRIP® COLLAR, 28MM, HA COATED | ELEOS Limb Salvage System With BioGrip | ONKOS SURGICAL, INC. |
7 | B278PB2400R03M0 | PB-2400R-03M | PB-2400R-03M | MODULAR POROUS BIOGRIP® COLLAR, 24MM, HA COATED | ELEOS Limb Salvage System With BioGrip | ONKOS SURGICAL, INC. |
8 | B278HR3000103M0 | HR-30001-03M | HR-30001-03M | ELEOS MODULAR COLLAR LOCKING RING AND IMPACTOR TIP | ELEOS Limb Salvage System | ONKOS SURGICAL, INC. |
9 | B278HR3000003M0 | HR-30000-03M | HR-30000-03M | ELEOS MODULAR COLLAR LOCKING RING | ELEOS Limb Salvage System | ONKOS SURGICAL, INC. |
10 | B278HC1712003M0 | HC-17120-03M | HC-17120-03M | SEGMENTAL COLLAR STEM, CEMENTED, 17MM X 100MM | ELEOS Limb Salvage System With BioGrip | ONKOS SURGICAL, INC. |
11 | B278HC1512003M0 | HC-15120-03M | HC-15120-03M | SEGMENTAL COLLAR STEM, CEMENTED, 15MM X 100MM | ELEOS Limb Salvage System With BioGrip | ONKOS SURGICAL, INC. |
12 | B278HC1312003M0 | HC-13120-03M | HC-13120-03M | SEGMENTAL COLLAR STEM, CEMENTED, 13MM X 100MM | ELEOS Limb Salvage System With BioGrip | ONKOS SURGICAL, INC. |
13 | B278HC1112003M0 | HC-11120-03M | HC-11120-03M | SEGMENTAL COLLAR STEM, CEMENTED, 11MM X 100MM | ELEOS Limb Salvage System With BioGrip | ONKOS SURGICAL, INC. |
14 | B278HC1010003M0 | HC-10100-03M | HC-10100-03M | SEGMENTAL COLLAR STEM, CEMENTED, 10MM X 100MM | ELEOS Limb Salvage System With BioGrip | ONKOS SURGICAL, INC. |
15 | B278HC0910003M0 | HC-09100-03M | HC-09100-03M | SEGMENTAL COLLAR STEM, CEMENTED, 9MM X 100MM | ELEOS Limb Salvage System With BioGrip | ONKOS SURGICAL, INC. |
16 | B278HB4000R03M0 | HB-4000R-03M | HB-4000R-03M | MODULAR POROUS BIOGRIP® COLLAR, 40MM, UNCOATED | ELEOS Limb Salvage System With BioGrip | ONKOS SURGICAL, INC. |
17 | B278HB3600R03M0 | HB-3600R-03M | HB-3600R-03M | MODULAR POROUS BIOGRIP® COLLAR, 36MM, UNCOATED | ELEOS Limb Salvage System With BioGrip | ONKOS SURGICAL, INC. |
18 | B278HB3200R03M0 | HB-3200R-03M | HB-3200R-03M | MODULAR POROUS BIOGRIP® COLLAR, 32MM, UNCOATED | ELEOS Limb Salvage System With BioGrip | ONKOS SURGICAL, INC. |
19 | B278HB2800R03M0 | HB-2800R-03M | HB-2800R-03M | MODULAR POROUS BIOGRIP® COLLAR, 28MM, UNCOATED | ELEOS Limb Salvage System With BioGrip | ONKOS SURGICAL, INC. |
20 | B278HB2400R03M0 | HB-2400R-03M | HB-2400R-03M | MODULAR POROUS BIOGRIP® COLLAR, 24MM, UNCOATED | ELEOS Limb Salvage System With BioGrip | ONKOS SURGICAL, INC. |
21 | 28031497000668 | SPC0522 | Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement coated onto a stainless steel reinforcing structure. The device is sterile and single-use. InterSpace Hip is indicated for temporary use (maximum of 180 days) as a total hip replacement (THR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. The device is inserted into the femoral medullary canal and acetabular cavity 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 Hip 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 Hip | TECRES SPA | |
22 | 28031497000651 | SPC0422 | Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement coated onto a stainless steel reinforcing structure. The device is sterile and single-use. InterSpace Hip is indicated for temporary use (maximum of 180 days) as a total hip replacement (THR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. The device is inserted into the femoral medullary canal and acetabular cavity 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 Hip 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 Hip | TECRES SPA | |
23 | 28031497000644 | SPC0322 | Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement coated onto a stainless steel reinforcing structure. The device is sterile and single-use. InterSpace Hip is indicated for temporary use (maximum of 180 days) as a total hip replacement (THR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. The device is inserted into the femoral medullary canal and acetabular cavity 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 Hip 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 Hip | TECRES SPA | |
24 | 28031497000637 | SPC0222 | Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement coated onto a stainless steel reinforcing structure. The device is sterile and single-use. InterSpace Hip is indicated for temporary use (maximum of 180 days) as a total hip replacement (THR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. The device is inserted into the femoral medullary canal and acetabular cavity 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 Hip 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 Hip | TECRES SPA | |
25 | 28031497000620 | SPC0122 | Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement coated onto a stainless steel reinforcing structure. The device is sterile and single-use. InterSpace Hip is indicated for temporary use (maximum of 180 days) as a total hip replacement (THR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. The device is inserted into the femoral medullary canal and acetabular cavity 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 Hip 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 Hip | TECRES SPA | |
26 | 28031497000613 | SPC0022 | Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cementcoated onto a stainless steel reinforcing structure. The device is sterile and single-use.InterSpace Hip is indicated for temporary use (maximum of 180 days) as a total hip replacement (THR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. The device is inserted into the femoral medullary canal and acetabular cavity 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 Hip 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 Hip | TECRES SPA | |
27 | 17613327311089 | I-H1236HA00 | I-H1236HA00 | SPECIALTY TRIDENT TRIAL CONTAINMENT SCREW-LONGER | INSTRUMENT | HOWMEDICA OSTEONICS CORP. |
28 | 17613327261100 | 0937-8-205 | 0937-8-205 | EXETER MIS HALF MOON FEMORAL CEMENT SEAL | INSTRUMENT | HOWMEDICA OSTEONICS CORP. |
29 | 17613327141358 | 0937-3-215 | 0937-3-215 | EXETER MIS HORSE COLLAR FEMORAL CEMENT SEAL | INSTRUMENT | HOWMEDICA OSTEONICS CORP. |
30 | 17613327141310 | 0937-3-225 | 0937-3-225 | EXETER MIS HORSE COLLAR FEMORAL CEMENT SEAL | INSTRUMENT | HOWMEDICA OSTEONICS CORP. |
31 | M7161112128590 | 111212859 | 111-21-2859 | Bipolar Head size 59 | OrthoMedFlex | ORTHOMEDFLEX LLC |
32 | M7161112128580 | 111212858 | 111-21-2858 | Bipolar Head size 58 | OrthoMedFlex | ORTHOMEDFLEX LLC |
33 | M7161112128570 | 111212857 | 111-21-2857 | Bipolar Head size 57 | OrthoMedFlex | ORTHOMEDFLEX LLC |
34 | M7161112128560 | 111212856 | 111-21-2856 | Bipolar Head size 56 | OrthoMedFlex | ORTHOMEDFLEX LLC |
35 | M7161112128550 | 111212855 | 111-21-2855 | Bipolar Head size 55 | OrthoMedFlex | ORTHOMEDFLEX LLC |
36 | M7161112128540 | 111212854 | 111-21-2854 | Bipolar Head size 54 | OrthoMedFlex | ORTHOMEDFLEX LLC |
37 | M7161112128530 | 111212853 | 111-21-2853 | Bipolar Head size 53 | OrthoMedFlex | ORTHOMEDFLEX LLC |
38 | M7161112128520 | 111212852 | 111-21-2852 | Bipolar Head size 52 | OrthoMedFlex | ORTHOMEDFLEX LLC |
39 | M7161112128510 | 111212851 | 111-21-2851 | Bipolar Head size 51 | OrthoMedFlex | ORTHOMEDFLEX LLC |
40 | M7161112128500 | 111212850 | 111-21-2850 | Bipolar Head size 50 | OrthoMedFlex | ORTHOMEDFLEX LLC |
41 | M7161112128490 | 111212849 | 111-21-2849 | Bipolar Head size 49 | OrthoMedFlex | ORTHOMEDFLEX LLC |
42 | M7161112128480 | 111212848 | 111-21-2848 | Bipolar Head size 48 | OrthoMedFlex | ORTHOMEDFLEX LLC |
43 | M7161112128470 | 111212847 | 111-21-2847 | Bipolar Head size 47 | OrthoMedFlex | ORTHOMEDFLEX LLC |
44 | M7161112128460 | 111212846 | 111-21-2846 | Bipolar Head size 46 | OrthoMedFlex | ORTHOMEDFLEX LLC |
45 | M7161112128450 | 111212845 | 111-21-2845 | Bipolar Head size 45 | OrthoMedFlex | ORTHOMEDFLEX LLC |
46 | M7161112128440 | 111212844 | 111-21-2844 | Bipolar Head size 44 | OrthoMedFlex | ORTHOMEDFLEX LLC |
47 | M7161112128430 | 111212843 | 111-21-2843 | Bipolar Head size 43 | OrthoMedFlex | ORTHOMEDFLEX LLC |
48 | M7161112128420 | 111212842 | 111-21-2842 | Bipolar Head size 42 | OrthoMedFlex | ORTHOMEDFLEX LLC |
49 | 10885862586834 | 01-001-01-0005 | 01-001-01-0005 | Alteon | EXACTECH, INC. | |
50 | 10885862586827 | 01-001-01-0004 | 01-001-01-0004 | Alteon | EXACTECH, INC. |