Other products from "ENDOTEC, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00814193020239 04-31-2106 04-31-2106 B-P KNEE MODULAR FEMORAL COMPONENT W/SCREW, W/BIOCOAT, W/ULTRACOAT, LEFT, SIZE 6 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
2 00814193020345 04-31-1206 04-31-1206 B-P KNEE TRICOMPARTMENTAL FEMORAL COMPONENT, W/O BIOCOAT, W/ULTRACOAT, RIGHT, SIZE 6 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
3 00814193020338 04-31-2205 04-31-2205 B-P KNEE TRICOMPARTMENTAL FEMORAL COMPONENT, W/O BIOCOAT, W/ULTRACOAT, LEFT, SIZE 5 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
4 00814193020321 04-31-1205 04-31-1205 B-P KNEE TRICOMPARTMENTAL FEMORAL COMPONENT, W/O BIOCOAT, W/ULTRACOAT, RIGHT, SIZE 5 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
5 00814193020314 04-31-2204 04-31-2204 B-P KNEE TRICOMPARTMENTAL FEMORAL COMPONENT, W/O BIOCOAT, W/ULTRACOAT, LEFT, SIZE 4 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
6 00814193020307 04-31-1204 04-31-1204 B-P KNEE TRICOMPARTMENTAL FEMORAL COMPONENT, W/O BIOCOAT, W/ULTRACOAT, RIGHT, SIZE 4 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
7 00814193020291 04-31-2203 04-31-2203 B-P KNEE TRICOMPARTMENTAL FEMORAL COMPONENT, W/O BIOCOAT, W/ULTRACOAT, LEFT, SIZE 3 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
8 00814193020284 04-31-1203 04-31-1203 B-P KNEE TRICOMPARTMENTAL FEMORAL COMPONENT, W/O BIOCOAT, W/ULTRACOAT, RIGHT, SIZE 3 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
9 00814193020277 04-31-2202 04-31-2202 B-P KNEE TRICOMPARTMENTAL FEMORAL COMPONENT, W/O BIOCOAT, W/ULTRACOAT, LEFT, SIZE 2 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
10 00814193020260 04-31-1202 04-31-1202 B-P KNEE TRICOMPARTMENTAL FEMORAL COMPONENT, W/O BIOCOAT, W/ULTRACOAT, RIGHT, SIZE 2 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
11 00814193020253 04-31-2201 04-31-2201 B-P KNEE TRICOMPARTMENTAL FEMORAL COMPONENT, W/O BIOCOAT, W/ULTRACOAT, LEFT, SIZE 1 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
12 00814193020246 04-31-1201 04-31-1201 B-P KNEE TRICOMPARTMENTAL FEMORAL COMPONENT, W/O BIOCOAT, W/ULTRACOAT, RIGHT, SIZE 1 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
13 00814193020222 04-31-1106 04-31-1106 B-P KNEE MODULAR FEMORAL COMPONENT W/SCREW, W/BIOCOAT, W/ULTRACOAT, RIGHT, SIZE 6 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
14 00814193020215 04-31-2105 04-31-2105 B-P KNEE MODULAR FEMORAL COMPONENT W/SCREW, W/BIOCOAT, W/ULTRACOAT, LEFT, SIZE 5 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
15 00814193020208 04-31-1105 04-31-1105 B-P KNEE MODULAR FEMORAL COMPONENT W/SCREW, W/BIOCOAT, W/ULTRACOAT, RIGHT, SIZE 5 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
16 00814193020192 04-31-2104 04-31-2104 B-P KNEE MODULAR FEMORAL COMPONENT W/SCREW, W/BIOCOAT, W/ULTRACOAT, LEFT, SIZE 4 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
17 00814193020185 04-31-1104 04-31-1104 B-P KNEE MODULAR FEMORAL COMPONENT W/SCREW, W/BIOCOAT, W/ULTRACOAT, RIGHT, SIZE 4 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
18 00814193020178 04-31-2103 04-31-2103 B-P KNEE MODULAR FEMORAL COMPONENT W/SCREW, W/BIOCOAT, W/ULTRACOAT, LEFT, SIZE 3 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
19 00814193020161 04-31-1103 04-31-1103 B-P KNEE MODULAR FEMORAL COMPONENT W/SCREW, W/BIOCOAT, W/ULTRACOAT, RIGHT, SIZE 3 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
20 00814193020154 04-31-2102 04-31-2102 B-P KNEE MODULAR FEMORAL COMPONENT W/SCREW, W/BIOCOAT, W/ULTRACOAT, LEFT, SIZE 2 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
21 00814193020147 04-31-1102 04-31-1102 B-P KNEE MODULAR FEMORAL COMPONENT W/SCREW, W/BIOCOAT, W/ULTRACOAT, RIGHT, SIZE 2 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
22 00814193020130 04-31-2101 04-31-2101 B-P KNEE MODULAR FEMORAL COMPONENT W/SCREW, W/BIOCOAT, W/ULTRACOAT, LEFT, SIZE 1 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
23 00814193020123 04-31-1101 04-31-1101 B-P KNEE MODULAR FEMORAL COMPONENT W/SCREW, W/BIOCOAT, W/ULTRACOAT, RIGHT, SIZE 1 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
24 00814193020116 04-31-2006 04-31-2006 B-P KNEE TRICOMPARTMENTAL FEMORAL COMPONENT, W/BIOCOAT, W/ULTRACOAT, LEFT, SIZE 6 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
25 00814193020109 04-31-1006 04-31-1006 B-P KNEE TRICOMPARTMENTAL FEMORAL COMPONENT, W/BIOCOAT, W/ULTRACOAT, RIGHT, SIZE 6 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
26 00814193020093 04-31-2005 04-31-2005 B-P KNEE TRICOMPARTMENTAL FEMORAL COMPONENT, W/BIOCOAT, W/ULTRACOAT, LEFT, SIZE 5 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
27 00814193020086 04-31-1005 04-31-1005 B-P KNEE TRICOMPARTMENTAL FEMORAL COMPONENT, W/BIOCOAT, W/ULTRACOAT, RIGHT, SIZE 5 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
28 00814193020079 04-31-2004 04-31-2004 B-P KNEE TRICOMPARTMENTAL FEMORAL COMPONENT, W/BIOCOAT, W/ULTRACOAT, LEFT, SIZE 4 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
29 00814193020062 04-31-1004 04-31-1004 B-P KNEE TRICOMPARTMENTAL FEMORAL COMPONENT, W/BIOCOAT, W/ULTRACOAT, RIGHT, SIZE 4 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
30 00814193020055 04-31-2003 04-31-2003 B-P KNEE TRICOMPARTMENTAL FEMORAL COMPONENT, W/BIOCOAT, W/ULTRACOAT, LEFT, SIZE 3 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
31 00814193020048 04-31-1003 04-31-1003 B-P KNEE TRICOMPARTMENTAL FEMORAL COMPONENT, W/BIOCOAT, W/ULTRACOAT, RIGHT, SIZE 3 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
32 00814193020031 04-31-2002 04-31-2002 B-P KNEE TRICOMPARTMENTAL FEMORAL COMPONENT, W/BIOCOAT, W/ULTRACOAT, LEFT, SIZE 2 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
33 00814193020024 04-31-1002 04-31-1002 B-P KNEE TRICOMPARTMENTAL FEMORAL COMPONENT, W/BIOCOAT, W/ULTRACOAT RIGHT, SIZE 2 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
34 00814193020017 04-31-2001 04-31-2001 B-P KNEE TRICOMPARTMENTAL FEMORAL COMPONENT, W/BIOCOAT, W/ULTRACOAT, LEFT, SIZE 1 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
35 00814193020000 04-31-1001 04-31-1001 B-P KNEE TRICOMPARTMENTAL FEMORAL COMPONENT, W/BIOCOAT, W/ULTRACOAT, RIGHT, SIZE 1 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
36 00814193020925 04-32-0113 04-32-0113 B-P KNEE MODULAR TIBIAL PLATFORM W/SCREW, W/BIOCOAT, W/ULTRACOAT, TYPE 2, SIZE 3 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
37 00814193020918 04-32-0112 04-32-0112 B-P KNEE MODULAR TIBIAL PLATFORM W/SCREW, W/BIOCOAT, W/ULTRACOAT, TYPE 2, SIZE 2 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
38 00814193020901 04-32-0111 04-32-0111 B-P KNEE MODULAR TIBIAL PLATFORM W/SCREW, W/BIOCOAT, W/ULTRACOAT, TYPE 2, SIZE 1 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
39 00814193020895 04-32-0106 04-32-0106 B-P KNEE MODULAR TIBIAL PLATFORM W/SCREW, W/BIOCOAT, W/ULTRACOAT, TYPE 1, SIZE 6 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
40 00814193020888 04-32-0105 04-32-0105 B-P KNEE MODULAR TIBIAL PLATFORM W/SCREW, W/BIOCOAT, W/ULTRACOAT, TYPE 1, SIZE 5 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
41 00814193020871 04-32-0104 04-32-0104 B-P KNEE MODULAR TIBIAL PLATFORM W/SCREW, W/BIOCOAT, W/ULTRACOAT, TYPE 1, SIZE 4 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
42 00814193020864 04-32-0103 04-32-0103 B-P KNEE MODULAR TIBIAL PLATFORM W/SCREW, W/BIOCOAT, W/ULTRACOAT, TYPE 1, SIZE 3 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
43 00814193020857 04-32-0102 04-32-0102 B-P KNEE MODULAR TIBIAL PLATFORM W/SCREW, W/BIOCOAT, W/ULTRACOAT, TYPE 1, SIZE 2 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
44 00814193020840 04-32-0101 04-32-0101 B-P KNEE MODULAR TIBIAL PLATFORM W/SCREW, W/BIOCOAT, W/ULTRACOAT, TYPE 1, SIZE 1 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
45 00814193020833 04-32-0066 04-32-0066 B-P KNEE TIBIA PLATFORM COMPONENT, W/BIOCOAT, W/ULTRACOAT, TYPE 0, SIZE 6 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
46 00814193020826 04-32-0065 04-32-0065 B-P KNEE TIBIA PLATFORM COMPONENT, W/BIOCOAT, W/ULTRACOAT, TYPE 0, SIZE 5 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
47 00814193020819 04-32-0064 04-32-0064 B-P KNEE TIBIA PLATFORM COMPONENT, W/BIOCOAT, W/ULTRACOAT, TYPE 0, SIZE 4 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
48 00814193020802 04-32-0063 04-32-0063 B-P KNEE TIBIA PLATFORM COMPONENT, W/BIOCOAT, W/ULTRACOAT, TYPE 0, SIZE 3 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
49 00814193020796 04-32-0062 04-32-0062 B-P KNEE TIBIA PLATFORM COMPONENT, W/BIOCOAT, W/ULTRACOAT, TYPE 0, SIZE 2 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
50 00814193020789 04-32-0061 04-32-0061 B-P KNEE TIBIA PLATFORM COMPONENT, W/BIOCOAT, W/ULTRACOAT, TYPE 0, SIZE 1 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 B-P TOTAL KNEE SYSTEM
Other products with the same Product Code "KWS"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 M528G2032520W0 G203-2520-W G203-2520-W ARTICULAR, 20 X 25MM IMPLANT, GLENOID 53/50 HEAD HemiCAPGRS® ARTHROSURFACE INCORPORATED
2 M528G2032520A0 G203-2520-A G203-2520-A ARTICULAR, 20 X 25MM IMPLANT, GLENOID 53/50 HEAD HemiCAPGRS® ARTHROSURFACE INCORPORATED
3 M528G2032515W0 G203-2515-W G203-2515-W ARTICULAR, 20 x 25mm IMPLANT, GLENOID 58/55 HEAD HemiCAPGRS® ARTHROSURFACE INCORPORATED
4 M528G2032515A0 G203-2515-A G203-2515-A ARTICULAR, 20 x 25mm IMPLANT, GLENOID 58/55 HEAD HemiCAPGRS® ARTHROSURFACE INCORPORATED
5 M528G2032015W0 G203-2015-W G203-2015-W ARTICULAR, 19 x 20mm IMPLANT, GLENOID 53/50 HEAD HemiCAPGRS® ARTHROSURFACE INCORPORATED
6 M528G2032015A0 G203-2015-A G203-2015-A ARTICULAR, 19 x 20mm IMPLANT, GLENOID 53/50 HEAD HemiCAPGRS® ARTHROSURFACE INCORPORATED
7 M528G2032010W0 G203-2010-W G203-2010-W ARTICULAR, 19 x 20mm IMPLANT, GLENOID 58/55 HEAD HemiCAPGRS® ARTHROSURFACE INCORPORATED
8 M528G2032010A0 G203-2010-A G203-2010-A ARTICULAR, 19 x 20mm IMPLANT, GLENOID 58/55 HEAD HemiCAPGRS® ARTHROSURFACE INCORPORATED
9 M528G00714000 G007-1400 G007-1400 Glenoid Pin Kit HemiCAPGRS® ARTHROSURFACE INCORPORATED
10 M528G00002000 G000-0200 G000-0200 Glenoid Universal Delivery Kit-Twin Glenoid HemiCAPGRS® ARTHROSURFACE INCORPORATED
11 M528G00001000 G000-0100 G000-0100 Glenoid Universal Delivery Kit HemiCAPGRS® ARTHROSURFACE INCORPORATED
12 M5288HM25854A0 8HM2-5854-A 8HM2-5854-A Humeral Component, 58mm x 54mm, OVOMotion OVOMotion™ ARTHROSURFACE INCORPORATED
13 M5288HM25652A0 8HM2-5652-A 8HM2-5652-A Humeral Component, 56mm x 52mm, OVOMotion OVOMotion™ ARTHROSURFACE INCORPORATED
14 M5288HM25450A0 8HM2-5450-A 8HM2-5450-A Humeral Component, 54mm x 50mm, OVOMotion OVOMotion™ ARTHROSURFACE INCORPORATED
15 M5288HM25248A0 8HM2-5248-A 8HM2-5248-A Humeral Component, 52mm x 48mm, OVOMotion OVOMotion™ ARTHROSURFACE INCORPORATED
16 M5288HM25046A0 8HM2-5046-A 8HM2-5046-A Humeral Component, 50mm x 46mm, OVOMotion OVOMotion™ ARTHROSURFACE INCORPORATED
17 M5288HM24844A0 8HM2-4844-A 8HM2-4844-A Humeral Component, 48mm x 44mm, OVOMotion OVOMotion™ ARTHROSURFACE INCORPORATED
18 M5288HM24642A0 8HM2-4642-A 8HM2-4642-A Humeral Component, 46mm x 42mm, OVOMotion OVOMotion™ ARTHROSURFACE INCORPORATED
19 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
20 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
21 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
22 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
23 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
24 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
25 08033390216418 9013.67.146 9013.67.146 PRIMA - Impactor Adaptor #6 PRIMA LIMACORPORATE SPA
26 08033390230599 9CCS.10.001 9CCS.10.001 ProMade shoulder 140° Reverse Resection Jig SMR Shoulder LIMACORPORATE SPA
27 08033390226172 9CCS.13.003 9CCS.13.003 Compactor S SMR Shoulder LIMACORPORATE SPA
28 08033390226165 9CCS.13.002 9CCS.13.002 Glenoid Drill Peg S SMR Shoulder LIMACORPORATE SPA
29 08033390216821 9013.67.067 9013.67.067 PRIMA - Metaphyseal Size ring #7 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 08033390216791 9013.67.065 9013.67.065 PRIMA - Metaphyseal Size ring #5 PRIMA LIMACORPORATE SPA
33 08033390216784 9013.67.063 9013.67.063 PRIMA - Metaphyseal Size ring #3 PRIMA LIMACORPORATE SPA
34 08033390216777 9013.67.062 9013.67.062 PRIMA - Metaphyseal Size ring #2 PRIMA LIMACORPORATE SPA
35 08033390216760 9013.67.061 9013.67.061 PRIMA - Metaphyseal Size ring #1 PRIMA LIMACORPORATE SPA
36 08033390216609 9013.67.140 9013.67.140 PRIMA - Impactor PRIMA LIMACORPORATE SPA
37 08033390216470 9013.67.141 9013.67.141 PRIMA - Impactor Adaptor #1 PRIMA LIMACORPORATE SPA
38 08033390216463 9013.67.055 9013.67.055 PRIMA - Metaphyseal Centering Guide - LEFT PRIMA LIMACORPORATE SPA
39 08033390216456 9013.67.050 9013.67.050 PRIMA - Metaphyseal Centering Guide - RIGHT PRIMA LIMACORPORATE SPA
40 08033390216432 9013.67.147 9013.67.147 PRIMA - Impactor Adaptor #7 PRIMA LIMACORPORATE SPA
41 08033390216401 9013.67.145 9013.67.145 PRIMA - Impactor Adaptor #5 PRIMA LIMACORPORATE SPA
42 08033390216395 9013.67.144 9013.67.144 PRIMA - Impactor Adaptor #4 PRIMA LIMACORPORATE SPA
43 08033390216333 9013.67.143 9013.67.143 PRIMA - Impactor Adaptor #3 PRIMA LIMACORPORATE SPA
44 08033390216326 9013.67.142 9013.67.142 PRIMA - Impactor Adaptor #2 PRIMA LIMACORPORATE SPA
45 08033390215763 9013.74.151 9013.74.151 SMR - Ecc. Glenosphere Orienter 42mm SMR Shoulder LIMACORPORATE SPA
46 08033390215756 9013.74.150 9013.74.150 SMR - Glenosphere Orienter 42mm SMR Shoulder LIMACORPORATE SPA
47 08033390214797 9013.67.020 9013.67.020 PRIMA - Humeral Starting Awl PRIMA LIMACORPORATE SPA
48 08033390214599 9013.79.583 9013.79.583 SMR Shoulder - Glenosph. Dia. 42-Ecc.42 Extract. Insert SMR Shoulder LIMACORPORATE SPA
49 08033390214582 9013.67.435 9013.67.435 PRIMA - Cemented Axial reamer #6-7 PRIMA LIMACORPORATE SPA
50 08033390214575 9013.67.427 9013.67.427 PRIMA - Cemented Axial reamer guide #7 PRIMA LIMACORPORATE SPA