Other products from "BIOPRO, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00810012485647 17180 LXH Orthopedic Manual Surgical Instrument 1 MPJ TRIAL 18.5mm (MS)
2 00810012484879 20519 HWC Screw, Fixation, Bone 2 HBS SCREW 3.0 X 16MM SDST
3 00810012485258 19751 HXX Screwdriver 1 HEX DRIVER 6.5
4 00810012485708 17368 LXH Orthopedic Manual Surgical Instrument 1 FIRST MPJ HEMI COMPLETE KIT
5 00810012482424 19688 HTY Pin, Fixation, Smooth 2 HBS KWIRE STERILE
6 00810012481977 19254 HWC Screw, Fixation, Bone 2 GOEZ SCREW 2.5 X 40MM
7 00810012480727 18166 HWC Screw, Fixation, Bone 2 GOEZ SCREW 2.0 X 14MM
8 00810012480338 17225 HWC Screw, Fixation, Bone 2 HORIZON TITANIUM SUBTALAR 12MM
9 M209223840 22384 HTY Pin, Fixation, Smooth 2 CURVED GUIDE WIRE SS
10 00810012485869 22648 HTY Pin, Fixation, Smooth 2 Horizon Subtalar Gen 2 - 12mm Implant
11 00810012485852 22647 HTY Pin, Fixation, Smooth 2 Horizon Subtalar Gen 2 - 11mm Implant
12 00810012484534 19572 HWC Screw, Fixation, Bone 2 3.0 x 16mm HBS Screw
13 00810012485814 22643 LXH Orthopedic Manual Surgical Instrument 1 Horizon Subtalar Gen 2 - 7mm Implant
14 00810012485807 22642 LXH Orthopedic Manual Surgical Instrument 1 Horizon Subtalar Gen 2 - 6mm Implant
15 00810012485753 22288 LXH Orthopedic Manual Surgical Instrument 1 GOEZ/HBS COMPLETE KIT
16 00810012485487 16963 LXH Orthopedic Manual Surgical Instrument 1 LESSER MPJ TRIAL 8.0MM
17 00810012485340 20044 LXH Orthopedic Manual Surgical Instrument 1 GOEZ SCREW INSTRUMENT TRAY
18 00810012485203 18400 LXH Orthopedic Manual Surgical Instrument 1 GOEZ SCREW INSTRUMENT TRAY
19 00810012484947 20526 HWC Screw, Fixation, Bone 2 HBS SCREW 3.0 X 30MM SDST
20 00810012484824 20514 HWC Screw, Fixation, Bone 2 HBS SCREW 2.5 X 38MM SDST
21 00810012484787 20510 HWC Screw, Fixation, Bone 2 HBS SCREW 2.5 X 30MM SDST
22 00810012484770 20509 HWC Screw, Fixation, Bone 2 HBS SCREW 2.5 X 28MM SDST
23 00810012484664 19585 HWC Screw, Fixation, Bone 2 3.0 x 29mm HBS Screw
24 00810012484497 19568 HWC Screw, Fixation, Bone 2 3.0 x 12mm HBS Screw
25 00810012484398 19558 HWC Screw, Fixation, Bone 2 2.5 x 23mm HBS Screw
26 00810012484244 19683 LXI Guide, Drill, Ligament 1 HBS DRILL COLLET ASSEMBLY STERILE
27 00810012484213 18880 LXH Orthopedic Manual Surgical Instrument 1 DEPTH GAUGE
28 00810012484152 18650 HWA Impactor 1 GUIDING HANDLE
29 00810012484114 18378 LXH Orthopedic Manual Surgical Instrument 1 DEPTH GAUGE
30 00810012483971 18300 LXH Orthopedic Manual Surgical Instrument 1 PUSHER 4 LEG 14X12
31 00810012483940 18297 FZX Guide, Surgical, Instrument 1 BURR GUIDE 4 LEG 14X12
32 00810012483933 18296 FZX Guide, Surgical, Instrument 1 BURR GUIDE 4 LEG 10X8
33 00810012483803 17651 LXH Orthopedic Manual Surgical Instrument 1 SM STAPLE 4 3/4 BULLDOG HEMO
34 00810012483780 17649 FZX Guide, Surgical, Instrument 1 DRILL GUIDE 11 13MM
35 00810012483469 OL25DBS HTW Bit, Drill 1 Drill bit AO QC 2.5 x 110/85mm, Sterile
36 00810012483407 OL20DBS HTW Bit, Drill 1 Drill bit AO QC 2.0 x 100/75mm, Sterile
37 00810012482141 19276 HWC Screw, Fixation, Bone 2 GOEZ SCREW 2.0 X 48MM
38 00810012483384 OL20010DS HTY Pin, Fixation, Smooth 2 Kwire double trocar 2.0 x 100mm, Sterile
39 00810012483285 OL15011S HTY Pin, Fixation, Smooth 2 Kwire single trocar 1.1 x 150mm, Sterile
40 00810012483186 95-8008C EMM Chisel, Osteotome, Surgical 1 OSTEOTOME, CURVED, 8MM
41 00810012483124 95-7423 EMM Chisel, Osteotome, Surgical 1 OSTEOTOME, BONE CEMENT, BEVELLED, CURVED, 310MM X 5MM
42 00810012482950 33.022.5200 HTY Pin, Fixation, Smooth 2 GUIDE WIRE, 2.5 X 200MM
43 00810012482226 19655 HWC Screw, Fixation, Bone 2 GOEZ SCREW 6.5 X 38MM
44 00810012482219 19654 HWC Screw, Fixation, Bone 2 GOEZ SCREW 6.5 X 36MM
45 00810012482080 19270 HWC Screw, Fixation, Bone 2 GOEZ SCREW 2.0 X 36MM
46 00810012482042 19266 HWC Screw, Fixation, Bone 2 GOEZ SCREW 2.0 X 28MM
47 00810012481823 19049 HWC Screw, Fixation, Bone 2 GOEZ SCREW 4.0 X 48MM
48 00810012481618 18262 JDR Staple, Fixation, Bone 2 CLOVER STAPLE 3 LEG 10 X 8 X 10
49 00810012481588 18071 JDR Staple, Fixation, Bone 2 Clover Staple 3 Leg 18mm x 16mm x 10mm
50 00810012481496 18243 HWC Screw, Fixation, Bone 2 GOEZ SCREW 4.5 X 14MM
Other products with the same Product Code "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
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.