Other products from "EXACTECH, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00817577023802 A 2000-7029 Syndesmosis Plate HRS Plate, Fixation, Bone 2 EPIC FRACTURE PLATE SYSTEM
2 00817577023796 A 2000-7028 Straight Plate Contoured - 14 Hole HRS Plate, Fixation, Bone 2 EPIC FRACTURE PLATE SYSTEM
3 00817577024823 A 2100-7001 Medial Hook Plate Drill Guide HRS Plate, Fixation, Bone 2 EPIC FRACTURE PLATE SYSTEM
4 00817577024816 A 2100-7000 Medial Hook Plate Impactor HRS Plate, Fixation, Bone 2 EPIC FRACTURE PLATE SYSTEM
5 00817577024342 A 2001-4060 4.0mm Non-Locking Screw x 60mm HRS Plate, Fixation, Bone 2 EPIC FRACTURE PLATE SYSTEM
6 00817577024311 A 2001-4055 4.0mm Non-Locking Screw x 55mm HRS Plate, Fixation, Bone 2 EPIC FRACTURE PLATE SYSTEM
7 00817577024281 A 2001-4050 4.0mm Non-Locking Screw x 50mm HRS Plate, Fixation, Bone 2 EPIC FRACTURE PLATE SYSTEM
8 00817577024250 A 2001-4045 4.0mm Non-Locking Screw x 45mm HRS Plate, Fixation, Bone 2 EPIC FRACTURE PLATE SYSTEM
9 00817577023789 A 2000-7027 Straight Plate Contoured - 12 Hole HRS Plate, Fixation, Bone 2 EPIC FRACTURE PLATE SYSTEM
10 00817577023772 A 2000-7026 Straight Plate Contoured - 10 Hole HRS Plate, Fixation, Bone 2 EPIC FRACTURE PLATE SYSTEM
11 00817577023765 A 2000-7025 Straight Plate Contoured - 8 Hole HRS Plate, Fixation, Bone 2 EPIC FRACTURE PLATE SYSTEM
12 00817577023758 A 2000-7024 Straight Plate Contoured - 6 Hole HRS Plate, Fixation, Bone 2 EPIC FRACTURE PLATE SYSTEM
13 00817577023741 A 2000-7023 Universal Recon Plate - 17 Hole HRS Plate, Fixation, Bone 2 EPIC FRACTURE PLATE SYSTEM
14 00817577023734 A 2000-7022 Universal Recon Plate - 15 Hole HRS Plate, Fixation, Bone 2 EPIC FRACTURE PLATE SYSTEM
15 00817577023727 A 2000-7021 Universal Recon Plate - 13 Hole HRS Plate, Fixation, Bone 2 EPIC FRACTURE PLATE SYSTEM
16 00817577023710 A 2000-7020 Universal Recon Plate - 11 Hole HRS Plate, Fixation, Bone 2 EPIC FRACTURE PLATE SYSTEM
17 00817577023703 A 2000-7019 Universal Recon Plate - 9 Hole HRS Plate, Fixation, Bone 2 EPIC FRACTURE PLATE SYSTEM
18 00817577023697 A 2000-7018 Straight Plate - 14 Hole HRS Plate, Fixation, Bone 2 EPIC FRACTURE PLATE SYSTEM
19 00817577023680 A 2000-7017 Straight Plate - 12 Hole HRS Plate, Fixation, Bone 2 EPIC FRACTURE PLATE SYSTEM
20 00817577023673 A 2000-7016 Straight Plate - 10 Hole HRS Plate, Fixation, Bone 2 EPIC FRACTURE PLATE SYSTEM
21 00817577023666 A 2000-7015 Straight Plate - 8 Hole HRS Plate, Fixation, Bone 2 EPIC FRACTURE PLATE SYSTEM
22 00817577023659 A 2000-7014 Straight Plate - 6 Hole HRS Plate, Fixation, Bone 2 EPIC FRACTURE PLATE SYSTEM
23 00817577023642 A 2000-7013 Posterior Plate - Long HRS Plate, Fixation, Bone 2 EPIC FRACTURE PLATE SYSTEM
24 00817577023635 A 2000-7012 Posterior Plate - Std HRS Plate, Fixation, Bone 2 EPIC FRACTURE PLATE SYSTEM
25 00817577023628 B 2000-7011 Left Lateral Fibula Plate - Xlong HRS Plate, Fixation, Bone 2 EPIC FRACTURE PLATE SYSTEM
26 00817577023611 B 2000-7010 Left Lateral Fibula Plate - Long HRS Plate, Fixation, Bone 2 EPIC FRACTURE PLATE SYSTEM
27 00817577023604 B 2000-7009 Left Lateral Fibula Plate - STD HRS Plate, Fixation, Bone 2 EPIC FRACTURE PLATE SYSTEM
28 00817577023598 B 2000-7008 Right Lateral Fibula Plate - XLong HRS Plate, Fixation, Bone 2 EPIC FRACTURE PLATE SYSTEM
29 00817577023581 B 2000-7007 Right Lateral Fibula Plate - Long HRS Plate, Fixation, Bone 2 EPIC FRACTURE PLATE SYSTEM
30 00817577023574 B 2000-7006 Right Lateral Fibula Plate - Std HRS Plate, Fixation, Bone 2 EPIC FRACTURE PLATE SYSTEM
31 00817577023567 B 2000-7005 Universal Lateral Fibula Plate - XLong HRS Plate, Fixation, Bone 2 EPIC FRACTURE PLATE SYSTEM
32 00817577023550 B 2000-7004 Universal Lateral Fibula Plate - Long HRS Plate, Fixation, Bone 2 EPIC FRACTURE PLATE SYSTEM
33 00817577023543 B 2000-7003 HRS Plate, Fixation, Bone 2 EPIC FRACTURE PLATE SYSTEM
34 00817577023536 A 2000-7002 HRS Plate, Fixation, Bone 2 EPIC FRACTURE PLATE SYSTEM
35 00817577023529 A 2000-7001 HRS Plate, Fixation, Bone 2 EPIC FRACTURE PLATE SYSTEM
36 00817577023512 1100-0005 1100-0005 RATCHET HANDLE, LARGE HXX SCREWDRIVER 1 NA
37 00817577023505 1100-0004 1100-0004 RATCHET HANDLE, SMALL HXX SCREWDRIVER 1 NA
38 00817577023208 4100-0001 4100-0001 SNAP-OFF DRIVER HWC Screw, fixation, bone 2 NA
39 00817577023130 2100-2700 2100-2700 2.7MM SOLID DRILL BIT HRS Plate, fixation, bone 2 NA
40 00817577022898 2100-2009 2100-2009 SPREADER (OPENING WEDGE) LXH Orthopedic manual surgical instrument 1 NA
41 00817577022881 2100-2027 2100-2027 2.0/2.7DOUBLEENDE DRILLGUIDE HRS Plate, fixation, bone 2 NA
42 00817577022874 2100-2000 2100-2000 2.0MM SOLID DRILL BIT HRS Plate, fixation, bone 2 NA
43 00817577022867 2100-1023 2100-1023 22MM CONE REAMER HTO REAMER 1 NA
44 00817577022850 2100-1022 2100-1022 22MM CUP REAMER HTO REAMER 1 NA
45 00817577022843 2100-1021 2100-1021 20MM CONE REAMER HTO REAMER 1 NA
46 00817577022836 2100-1020 2100-1020 20MM CUP REAMER HTO REAMER 1 NA
47 00817577022829 2100-1019 2100-1019 18MM CONE REAMER HTO REAMER 1 NA
48 00817577022812 2100-1018 2100-1018 18MM CUP REAMER HTO REAMER 1 NA
49 00817577022805 2100-1017 2100-1017 16MM CONE REAMER HTO REAMER 1 NA
50 00817577022799 2100-1016 2100-1016 16MM CUP REAMER HTO REAMER 1 NA
Other products with the same Product Code "KWY"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 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
2 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
3 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
4 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
5 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
6 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
7 17613327311089 I-H1236HA00 I-H1236HA00 SPECIALTY TRIDENT TRIAL CONTAINMENT SCREW-LONGER INSTRUMENT HOWMEDICA OSTEONICS CORP.
8 17613327261100 0937-8-205 0937-8-205 EXETER MIS HALF MOON FEMORAL CEMENT SEAL INSTRUMENT HOWMEDICA OSTEONICS CORP.
9 17613327141358 0937-3-215 0937-3-215 EXETER MIS HORSE COLLAR FEMORAL CEMENT SEAL INSTRUMENT HOWMEDICA OSTEONICS CORP.
10 17613327141310 0937-3-225 0937-3-225 EXETER MIS HORSE COLLAR FEMORAL CEMENT SEAL INSTRUMENT HOWMEDICA OSTEONICS CORP.
11 M7161112128590 111212859 111-21-2859 Bipolar Head size 59 OrthoMedFlex ORTHOMEDFLEX LLC
12 M7161112128580 111212858 111-21-2858 Bipolar Head size 58 OrthoMedFlex ORTHOMEDFLEX LLC
13 M7161112128570 111212857 111-21-2857 Bipolar Head size 57 OrthoMedFlex ORTHOMEDFLEX LLC
14 M7161112128560 111212856 111-21-2856 Bipolar Head size 56 OrthoMedFlex ORTHOMEDFLEX LLC
15 M7161112128550 111212855 111-21-2855 Bipolar Head size 55 OrthoMedFlex ORTHOMEDFLEX LLC
16 M7161112128540 111212854 111-21-2854 Bipolar Head size 54 OrthoMedFlex ORTHOMEDFLEX LLC
17 M7161112128530 111212853 111-21-2853 Bipolar Head size 53 OrthoMedFlex ORTHOMEDFLEX LLC
18 M7161112128520 111212852 111-21-2852 Bipolar Head size 52 OrthoMedFlex ORTHOMEDFLEX LLC
19 M7161112128510 111212851 111-21-2851 Bipolar Head size 51 OrthoMedFlex ORTHOMEDFLEX LLC
20 M7161112128500 111212850 111-21-2850 Bipolar Head size 50 OrthoMedFlex ORTHOMEDFLEX LLC
21 M7161112128490 111212849 111-21-2849 Bipolar Head size 49 OrthoMedFlex ORTHOMEDFLEX LLC
22 M7161112128480 111212848 111-21-2848 Bipolar Head size 48 OrthoMedFlex ORTHOMEDFLEX LLC
23 M7161112128470 111212847 111-21-2847 Bipolar Head size 47 OrthoMedFlex ORTHOMEDFLEX LLC
24 M7161112128460 111212846 111-21-2846 Bipolar Head size 46 OrthoMedFlex ORTHOMEDFLEX LLC
25 M7161112128450 111212845 111-21-2845 Bipolar Head size 45 OrthoMedFlex ORTHOMEDFLEX LLC
26 M7161112128440 111212844 111-21-2844 Bipolar Head size 44 OrthoMedFlex ORTHOMEDFLEX LLC
27 M7161112128430 111212843 111-21-2843 Bipolar Head size 43 OrthoMedFlex ORTHOMEDFLEX LLC
28 M7161112128420 111212842 111-21-2842 Bipolar Head size 42 OrthoMedFlex ORTHOMEDFLEX LLC
29 10885862586834 01-001-01-0005 01-001-01-0005 Alteon EXACTECH, INC.
30 10885862586827 01-001-01-0004 01-001-01-0004 Alteon EXACTECH, INC.
31 10885862536174 01-003-04-0009 01-003-04-0009 CALCAR PLANER BLADE 1" NA EXACTECH, INC.
32 10885862535894 01-003-04-0008 01-003-04-0008 CALCAR PLANER BLADE 1.3" NA EXACTECH, INC.
33 10885862534088 01-003-06-0008 01-003-06-0008 CANAL FINDER, TOOTHED STARTER BROACH NA EXACTECH, INC.
34 10885862530103 01-003-02-0007 01-003-02-0007 DUAL OFFSET BROACH HANDLE, RIGHT, NO TWIST NA EXACTECH, INC.
35 10885862530097 01-003-02-0006 01-003-02-0006 DUAL OFFSET BROACH HANDLE, LEFT, NO TWIST NA EXACTECH, INC.
36 10885862528490 190-61-15 190-61-15 Alteon Highly Polished Femoral Stem Alteon EXACTECH, INC.
37 10885862528483 190-61-14 190-61-14 Alteon Highly Polished Femoral Stem Alteon EXACTECH, INC.
38 10885862528476 190-61-13 190-61-13 Alteon Highly Polished Femoral Stem Alteon EXACTECH, INC.
39 10885862528469 190-61-11 190-61-11 Alteon Highly Polished Femoral Stem Alteon EXACTECH, INC.
40 10885862528452 190-61-09 190-61-09 Alteon Highly Polished Femoral Stem Alteon EXACTECH, INC.
41 10885862528445 190-61-07 190-61-07 Alteon Highly Polished Femoral Stem Alteon EXACTECH, INC.
42 10885862528438 190-61-05 190-61-05 Alteon Highly Polished Femoral Stem Alteon EXACTECH, INC.
43 10885862528421 190-60-15 190-60-15 Alteon Highly Polished Femoral Stem Alteon EXACTECH, INC.
44 10885862528414 190-60-14 190-60-14 Alteon Highly Polished Femoral Stem Alteon EXACTECH, INC.
45 10885862528407 190-60-13 190-60-13 Alteon Highly Polished Femoral Stem Alteon EXACTECH, INC.
46 10885862528391 190-60-11 190-60-11 Alteon Highly Polished Femoral Stem Alteon EXACTECH, INC.
47 10885862528384 190-60-09 190-60-09 Alteon Highly Polished Femoral Stem Alteon EXACTECH, INC.
48 10885862528377 190-60-07 190-60-07 Alteon Highly Polished Femoral Stem Alteon EXACTECH, INC.
49 10885862528360 190-60-05 190-60-05 Alteon Highly Polished Femoral Stem Alteon EXACTECH, INC.
50 10885862527028 190-61-12 190-61-12 Alteon Highly Polished Femoral Stem Alteon EXACTECH, INC.