Other products from "ORTHOSOFT INC"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00889024304536 20-8000-010-30 20-8000-010-30 HAW Neurological Stereotaxic Instrument 2 NA
2 00889024304529 20-8000-010-29 20-8000-010-29 OLO,HAW Orthopedic Stereotaxic Instrument,Neurological Stereotaxic Instrument 2 NA
3 00889024304512 20-8000-010-28 20-8000-010-28 HAW,OLO Neurological Stereotaxic Instrument,Orthopedic Stereotaxic Instrument 2 NA
4 00889024304505 20-8000-010-27 20-8000-010-27 HAW,OLO Neurological Stereotaxic Instrument,Orthopedic Stereotaxic Instrument 2 NA
5 00889024304499 20-8000-010-26 20-8000-010-26 OLO,HAW Orthopedic Stereotaxic Instrument,Neurological Stereotaxic Instrument 2 NA
6 00889024304482 20-8000-010-25 20-8000-010-25 OLO,HAW Orthopedic Stereotaxic Instrument,Neurological Stereotaxic Instrument 2 NA
7 00889024304475 20-8000-010-24 20-8000-010-24 OLO,HAW Orthopedic Stereotaxic Instrument,Neurological Stereotaxic Instrument 2 NA
8 00889024304468 20-8000-010-23 20-8000-010-23 HAW,OLO Neurological Stereotaxic Instrument,Orthopedic Stereotaxic Instrument 2 NA
9 00889024304451 20-8000-010-22 20-8000-010-22 OLO,HAW Orthopedic Stereotaxic Instrument,Neurological Stereotaxic Instrument 2 NA
10 00889024304437 20-8000-010-20 20-8000-010-20 OLO,HAW Orthopedic Stereotaxic Instrument,Neurological Stereotaxic Instrument 2 NA
11 00889024304420 20-8000-010-19 20-8000-010-19 OLO,HAW Orthopedic Stereotaxic Instrument,Neurological Stereotaxic Instrument 2 NA
12 00889024304413 20-8000-010-18 20-8000-010-18 OLO,HAW Orthopedic Stereotaxic Instrument,Neurological Stereotaxic Instrument 2 NA
13 00889024304406 20-8000-010-17 20-8000-010-17 OLO,HAW Orthopedic Stereotaxic Instrument,Neurological Stereotaxic Instrument 2 NA
14 00889024304376 20-8000-010-14 20-8000-010-14 OLO,HAW Orthopedic Stereotaxic Instrument,Neurological Stereotaxic Instrument 2 NA
15 00889024304369 20-8000-010-13 20-8000-010-13 OLO,HAW Orthopedic Stereotaxic Instrument,Neurological Stereotaxic Instrument 2 NA
16 00889024304352 20-8000-010-12 20-8000-010-12 HAW,OLO Neurological Stereotaxic Instrument,Orthopedic Stereotaxic Instrument 2 NA
17 00889024304345 20-8000-010-11 20-8000-010-11 HAW,OLO Neurological Stereotaxic Instrument,Orthopedic Stereotaxic Instrument 2 NA
18 00889024304321 20-8000-010-09 20-8000-010-09 OLO,HAW Orthopedic Stereotaxic Instrument,Neurological Stereotaxic Instrument 2 NA
19 00889024304314 20-8000-010-07 20-8000-010-07 OLO,HAW Orthopedic Stereotaxic Instrument,Neurological Stereotaxic Instrument 2 NA
20 00889024304291 20-8000-010-01 20-8000-010-01 HAW,OLO Neurological Stereotaxic Instrument,Orthopedic Stereotaxic Instrument 2 NA
21 00889024305304 20-8011-020-00 20-8011-020-00 OLO Orthopedic Stereotaxic Instrument 2 NA
22 00889024305298 20-8011-019-00 20-8011-019-00 OLO Orthopedic Stereotaxic Instrument 2 NA
23 00889024305281 20-8011-018-00 20-8011-018-00 OLO Orthopedic Stereotaxic Instrument 2 NA
24 00889024305380 20-8011-028-50 20-8011-028-50 OLO Orthopedic Stereotaxic Instrument 2 NA
25 00889024305373 20-8011-028-00 20-8011-028-00 OLO Orthopedic Stereotaxic Instrument 2 NA
26 00889024305366 20-8011-027-50 20-8011-027-50 OLO Orthopedic Stereotaxic Instrument 2 NA
27 00889024305359 20-8011-027-00 20-8011-027-00 OLO Orthopedic Stereotaxic Instrument 2 NA
28 00889024305342 20-8011-026-00 20-8011-026-00 OLO Orthopedic Stereotaxic Instrument 2 NA
29 00889024305335 20-8011-025-00 20-8011-025-00 OLO Orthopedic Stereotaxic Instrument 2 NA
30 00889024492714 20-8011-013-01 OLO Orthopedic Stereotaxic Instrument 2 NA
31 00889024492707 20-8000-000-21 OLO Orthopedic Stereotaxic Instrument 2 NA
32 00889024492691 20-8000-000-15 OLO Orthopedic Stereotaxic Instrument 2 NA
33 00889024305311 20-8011-021-00 20-8011-021-00 OLO Orthopedic Stereotaxic Instrument 2 NA
34 00889024305274 20-8011-017-00 20-8011-017-00 OLO Orthopedic Stereotaxic Instrument 2 NA
35 00889024492660 20-8000-020-27 HAW Neurological Stereotaxic Instrument 2 NA
36 00889024479012 20-8000-080-11 OLO Orthopedic Stereotaxic Instrument 2 NA
37 00889024479005 20-8000-080-10 OLO Orthopedic Stereotaxic Instrument 2 NA
38 00889024305267 20-8011-013-00 20-8011-013-00 OLO Orthopedic Stereotaxic Instrument 2 NA
39 00889024304840 20-8000-020-10 20-8000-020-10 HAW Neurological Stereotaxic Instrument 2 NA
40 00889024305410 20-8011-042-00 20-8011-042-00 OLO Orthopedic Stereotaxic Instrument 2 NA
41 00889024304888 20-8000-020-14 20-8000-020-14 HAW Neurological Stereotaxic Instrument 2 NA
42 00889024304871 20-8000-020-13 20-8000-020-13 HAW Neurological Stereotaxic Instrument 2 NA
43 00889024304598 20-8000-010-37 20-8000-010-37 OLO,HAW Orthopedic Stereotaxic Instrument,Neurological Stereotaxic Instrument 2 NA
44 00889024305564 20-8014-014-00 20-8014-014-00 OOG,MBH,JWH Knee Arthroplasty Implantation System,Prosthesis, Knee, Patello/Femorotibial, Se Knee Arthroplasty Implantation System,Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer,Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 NA
45 00889024304574 20-8000-010-35 20-8000-010-35 OLO,HAW Orthopedic Stereotaxic Instrument,Neurological Stereotaxic Instrument 2 NA
46 00889024305526 20-8011-070-03 20-8011-070-03 HAW Neurological Stereotaxic Instrument 2 NA
47 00889024305519 20-8011-070-02 20-8011-070-02 HAW Neurological Stereotaxic Instrument 2 NA
48 00889024305465 20-8011-056-52 20-8011-056-52 OLO Orthopedic Stereotaxic Instrument 2 NA
49 00889024304857 20-8000-020-11 20-8000-020-11 HAW Neurological Stereotaxic Instrument 2 NA
50 00889024305458 20-8011-056-51 20-8011-056-51 OLO Orthopedic Stereotaxic Instrument 2 NA
Other products with the same Product Codes "QHE, KWT, KWS, PHX, MBF"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 08058964726087 900001 144818 "Disposable cement spacer molds with metal reinforcement stem are indicated for "Disposable cement spacer molds with metal reinforcement stem are indicated for use to mold atemporary hemi- shoulder replacement for skeletally mature patients undergoing a two-stagerevision procedure due to a septic process.The temporary prosthesis is molded using low viscosity polymethylmethacrylate bonecement and inserted into the humeral medullary canal and glenoid cavity of the shoulderfollowing removal of the existing humeral and glenoideal cavity implants and debridement.SpaceFlex Shoulder should only be used with G3A low-viscosity bone cement.The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy(standard treatment approach to an infection).The hemi-shoulder prosthesis made from the SpaceFlex Shoulder disposable cement molds isnot intended for use more than 180 days, at which time it must be explanted and permanentdevices implanted or another appropriate treatment performed (e.g. resection arthroplasty,fusion, etc.).Due to the inherent mechanical limitations of the hemi-shoulder prosthesis material (lowviscosity polymethylmethacrylate), the temporary hemi-shoulder prosthesis is only indicatedfor patients who will consistently follow activity limitation throughout the implant period.The device can exclusively be used by competent healthcare personnel who has completescientific and anatomical knowledge." SpaceFlex Shoulder G21 SRL
2 08058964726070 900001 124818 Disposable cement spacer molds with metal reinforcement stem are indicated for u Disposable cement spacer molds with metal reinforcement stem are indicated for use to mold atemporary hemi- shoulder replacement for skeletally mature patients undergoing a two-stagerevision procedure due to a septic process.The temporary prosthesis is molded using low viscosity polymethylmethacrylate bonecement and inserted into the humeral medullary canal and glenoid cavity of the shoulderfollowing removal of the existing humeral and glenoideal cavity implants and debridement.SpaceFlex Shoulder should only be used with G3A low-viscosity bone cement.The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy(standard treatment approach to an infection).The hemi-shoulder prosthesis made from the SpaceFlex Shoulder disposable cement molds isnot intended for use more than 180 days, at which time it must be explanted and permanentdevices implanted or another appropriate treatment performed (e.g. resection arthroplasty,fusion, etc.).Due to the inherent mechanical limitations of the hemi-shoulder prosthesis material (lowviscosity polymethylmethacrylate), the temporary hemi-shoulder prosthesis is only indicatedfor patients who will consistently follow activity limitation throughout the implant period.The device can exclusively be used by competent healthcare personnel who has completescientific and anatomical knowledge. SpaceFlex Shoulder G21 SRL
3 08058964726063 900001 124215 Disposable cement spacer molds with metal reinforcement stem are indicated for u Disposable cement spacer molds with metal reinforcement stem are indicated for use to mold atemporary hemi- shoulder replacement for skeletally mature patients undergoing a two-stagerevision procedure due to a septic process.The temporary prosthesis is molded using low viscosity polymethylmethacrylate bonecement and inserted into the humeral medullary canal and glenoid cavity of the shoulderfollowing removal of the existing humeral and glenoideal cavity implants and debridement.SpaceFlex Shoulder should only be used with G3A low-viscosity bone cement.The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy(standard treatment approach to an infection).The hemi-shoulder prosthesis made from the SpaceFlex Shoulder disposable cement molds isnot intended for use more than 180 days, at which time it must be explanted and permanentdevices implanted or another appropriate treatment performed (e.g. resection arthroplasty,fusion, etc.).Due to the inherent mechanical limitations of the hemi-shoulder prosthesis material (lowviscosity polymethylmethacrylate), the temporary hemi-shoulder prosthesis is only indicatedfor patients who will consistently follow activity limitation throughout the implant period.The device can exclusively be used by competent healthcare personnel who has completescientific and anatomical knowledge. SpaceFlex Shoulder G21 SRL
4 08058964726056 900001 104818 Disposable cement spacer molds with metal reinforcement stem are indicated for u Disposable cement spacer molds with metal reinforcement stem are indicated for use to mold atemporary hemi- shoulder replacement for skeletally mature patients undergoing a two-stagerevision procedure due to a septic process.The temporary prosthesis is molded using low viscosity polymethylmethacrylate bonecement and inserted into the humeral medullary canal and glenoid cavity of the shoulderfollowing removal of the existing humeral and glenoideal cavity implants and debridement.SpaceFlex Shoulder should only be used with G3A low-viscosity bone cement.The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy(standard treatment approach to an infection).The hemi-shoulder prosthesis made from the SpaceFlex Shoulder disposable cement molds isnot intended for use more than 180 days, at which time it must be explanted and permanentdevices implanted or another appropriate treatment performed (e.g. resection arthroplasty,fusion, etc.).Due to the inherent mechanical limitations of the hemi-shoulder prosthesis material (lowviscosity polymethylmethacrylate), the temporary hemi-shoulder prosthesis is only indicatedfor patients who will consistently follow activity limitation throughout the implant period.The device can exclusively be used by competent healthcare personnel who has completescientific and anatomical knowledge. SpaceFlex Shoulder G21 SRL
5 08058964726049 900001 104215 Disposable cement spacer molds with metal reinforcement stem are indicated for u Disposable cement spacer molds with metal reinforcement stem are indicated for use to mold atemporary hemi- shoulder replacement for skeletally mature patients undergoing a two-stagerevision procedure due to a septic process.The temporary prosthesis is molded using low viscosity polymethylmethacrylate bonecement and inserted into the humeral medullary canal and glenoid cavity of the shoulderfollowing removal of the existing humeral and glenoideal cavity implants and debridement.SpaceFlex Shoulder should only be used with G3A low-viscosity bone cement.The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy(standard treatment approach to an infection).The hemi-shoulder prosthesis made from the SpaceFlex Shoulder disposable cement molds isnot intended for use more than 180 days, at which time it must be explanted and permanentdevices implanted or another appropriate treatment performed (e.g. resection arthroplasty,fusion, etc.).Due to the inherent mechanical limitations of the hemi-shoulder prosthesis material (lowviscosity polymethylmethacrylate), the temporary hemi-shoulder prosthesis is only indicatedfor patients who will consistently follow activity limitation throughout the implant period.The device can exclusively be used by competent healthcare personnel who has completescientific and anatomical knowledge. SpaceFlex Shoulder G21 SRL
6 08058964724977 900001 084215 Disposable cement spacer molds with metal reinforcement stem are indicated for u Disposable cement spacer molds with metal reinforcement stem are indicated for use to mold atemporary hemi- shoulder replacement for skeletally mature patients undergoing a two-stagerevision procedure due to a septic process.The temporary prosthesis is molded using low viscosity polymethylmethacrylate bonecement and inserted into the humeral medullary canal and glenoid cavity of the shoulderfollowing removal of the existing humeral and glenoideal cavity implants and debridement.SpaceFlex Shoulder should only be used with G3A low-viscosity bone cement.The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy(standard treatment approach to an infection).The hemi-shoulder prosthesis made from the SpaceFlex Shoulder disposable cement molds isnot intended for use more than 180 days, at which time it must be explanted and permanentdevices implanted or another appropriate treatment performed (e.g. resection arthroplasty,fusion, etc.).Due to the inherent mechanical limitations of the hemi-shoulder prosthesis material (lowviscosity polymethylmethacrylate), the temporary hemi-shoulder prosthesis is only indicatedfor patients who will consistently follow activity limitation throughout the implant period.The device can exclusively be used by competent healthcare personnel who has completescientific and anatomical knowledge. SpaceFlex Shoulder G21 SRL
7 08033390216418 9013.67.146 9013.67.146 PRIMA - Impactor Adaptor #6 PRIMA LIMACORPORATE SPA
8 08033390244640 9CC0.13.03B 9CC0.13.03B Glenoid Drilling Guide Dia. 2,7 mm ProMade LIMACORPORATE SPA
9 08033390237420 9CC0.13.03E 9CC0.13.03E M8 Long Handle ProMade LIMACORPORATE SPA
10 08033390237406 9CC0.13.03C 9CC0.13.03C M8 Handle with Flange ProMade LIMACORPORATE SPA
11 08033390237338 9CC0.13.038 9CC0.13.038 Glenoid Drilling Guide - Dia. 3.2 mm Drill ProMade LIMACORPORATE SPA
12 08033390216418 9013.67.146 9013.67.146 PRIMA - Impactor Adaptor #6 PRIMA LIMACORPORATE SPA
13 08033390230599 9CCS.10.001 9CCS.10.001 ProMade shoulder 140° Reverse Resection Jig SMR Shoulder LIMACORPORATE SPA
14 08033390230599 9CCS.10.001 9CCS.10.001 ProMade shoulder 140° Reverse Resection Jig SMR Shoulder LIMACORPORATE SPA
15 08033390230599 9CCS.10.001 9CCS.10.001 ProMade shoulder 140° Reverse Resection Jig SMR Shoulder LIMACORPORATE SPA
16 08033390230599 9CCS.10.001 9CCS.10.001 ProMade shoulder 140° Reverse Resection Jig SMR Shoulder LIMACORPORATE SPA
17 08033390226172 9CCS.13.003 9CCS.13.003 Compactor S SMR Shoulder LIMACORPORATE SPA
18 08033390226172 9CCS.13.003 9CCS.13.003 Compactor S SMR Shoulder LIMACORPORATE SPA
19 08033390226172 9CCS.13.003 9CCS.13.003 Compactor S SMR Shoulder LIMACORPORATE SPA
20 08033390226172 9CCS.13.003 9CCS.13.003 Compactor S SMR Shoulder LIMACORPORATE SPA
21 08033390226165 9CCS.13.002 9CCS.13.002 Glenoid Drill Peg S SMR Shoulder LIMACORPORATE SPA
22 08033390226165 9CCS.13.002 9CCS.13.002 Glenoid Drill Peg S SMR Shoulder LIMACORPORATE SPA
23 08033390226165 9CCS.13.002 9CCS.13.002 Glenoid Drill Peg S SMR Shoulder LIMACORPORATE SPA
24 08033390226165 9CCS.13.002 9CCS.13.002 Glenoid Drill Peg S SMR Shoulder LIMACORPORATE SPA
25 08033390216821 9013.67.067 9013.67.067 PRIMA - Metaphyseal Size ring #7 PRIMA LIMACORPORATE SPA
26 08033390216821 9013.67.067 9013.67.067 PRIMA - Metaphyseal Size ring #7 PRIMA LIMACORPORATE SPA
27 08033390216821 9013.67.067 9013.67.067 PRIMA - Metaphyseal Size ring #7 PRIMA LIMACORPORATE SPA
28 08033390216814 9013.67.066 9013.67.066 PRIMA - Metaphyseal Size ring #6 PRIMA LIMACORPORATE SPA
29 08033390216814 9013.67.066 9013.67.066 PRIMA - Metaphyseal Size ring #6 PRIMA LIMACORPORATE SPA
30 08033390216814 9013.67.066 9013.67.066 PRIMA - Metaphyseal Size ring #6 PRIMA LIMACORPORATE SPA
31 08033390216807 9013.67.064 9013.67.064 PRIMA - Metaphyseal Size ring #4 PRIMA LIMACORPORATE SPA
32 08033390216807 9013.67.064 9013.67.064 PRIMA - Metaphyseal Size ring #4 PRIMA LIMACORPORATE SPA
33 08033390216807 9013.67.064 9013.67.064 PRIMA - Metaphyseal Size ring #4 PRIMA LIMACORPORATE SPA
34 08033390216791 9013.67.065 9013.67.065 PRIMA - Metaphyseal Size ring #5 PRIMA LIMACORPORATE SPA
35 08033390216791 9013.67.065 9013.67.065 PRIMA - Metaphyseal Size ring #5 PRIMA LIMACORPORATE SPA
36 08033390216791 9013.67.065 9013.67.065 PRIMA - Metaphyseal Size ring #5 PRIMA LIMACORPORATE SPA
37 08033390216784 9013.67.063 9013.67.063 PRIMA - Metaphyseal Size ring #3 PRIMA LIMACORPORATE SPA
38 08033390216784 9013.67.063 9013.67.063 PRIMA - Metaphyseal Size ring #3 PRIMA LIMACORPORATE SPA
39 08033390216784 9013.67.063 9013.67.063 PRIMA - Metaphyseal Size ring #3 PRIMA LIMACORPORATE SPA
40 08033390216777 9013.67.062 9013.67.062 PRIMA - Metaphyseal Size ring #2 PRIMA LIMACORPORATE SPA
41 08033390216777 9013.67.062 9013.67.062 PRIMA - Metaphyseal Size ring #2 PRIMA LIMACORPORATE SPA
42 08033390216777 9013.67.062 9013.67.062 PRIMA - Metaphyseal Size ring #2 PRIMA LIMACORPORATE SPA
43 08033390216760 9013.67.061 9013.67.061 PRIMA - Metaphyseal Size ring #1 PRIMA LIMACORPORATE SPA
44 08033390216760 9013.67.061 9013.67.061 PRIMA - Metaphyseal Size ring #1 PRIMA LIMACORPORATE SPA
45 08033390216760 9013.67.061 9013.67.061 PRIMA - Metaphyseal Size ring #1 PRIMA LIMACORPORATE SPA
46 08033390216609 9013.67.140 9013.67.140 PRIMA - Impactor PRIMA LIMACORPORATE SPA
47 08033390216609 9013.67.140 9013.67.140 PRIMA - Impactor PRIMA LIMACORPORATE SPA
48 08033390216609 9013.67.140 9013.67.140 PRIMA - Impactor PRIMA LIMACORPORATE SPA
49 08033390216470 9013.67.141 9013.67.141 PRIMA - Impactor Adaptor #1 PRIMA LIMACORPORATE SPA
50 08033390216470 9013.67.141 9013.67.141 PRIMA - Impactor Adaptor #1 PRIMA LIMACORPORATE SPA