Other products from "WRIGHT MEDICAL TECHNOLOGY, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00889797102520 RR2000 RR2000 KTT APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT 2 NA
2 00889797102513 RR1200 RR1200 JDW,KTT PIN, FIXATION, THREADED,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTI PIN, FIXATION, THREADED,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT 2 NA
3 00840420163493 SB170150 SB170150 HWC Screw, fixation, bone 2 SALVATION
4 00840420163486 SB170145 SB170145 HWC Screw, fixation, bone 2 SALVATION
5 00840420163479 SB170140 SB170140 HWC Screw, fixation, bone 2 SALVATION
6 00840420163462 SB170135 SB170135 HWC Screw, fixation, bone 2 SALVATION
7 00840420163455 SB170130 SB170130 HWC Screw, fixation, bone 2 SALVATION
8 00840420163448 SB170125 SB170125 HWC Screw, fixation, bone 2 SALVATION
9 00840420163431 SB170120 SB170120 HWC Screw, fixation, bone 2 SALVATION
10 00840420163400 SB170105 SB170105 HWC Screw, fixation, bone 2 SALVATION
11 00840420163394 SB170100 SB170100 HWC Screw, fixation, bone 2 SALVATION
12 00840420163387 SB017095 SB017095 HWC Screw, fixation, bone 2 SALVATION
13 00840420163363 SB017085 SB017085 HWC Screw, fixation, bone 2 SALVATION
14 00840420163356 SB017080 SB017080 HWC Screw, fixation, bone 2 SALVATION
15 00840420163349 SB017075 SB017075 HWC Screw, fixation, bone 2 SALVATION
16 00840420163332 SB017070 SB017070 HWC Screw, fixation, bone 2 SALVATION
17 00840420163325 SB017065 SB017065 HWC Screw, fixation, bone 2 SALVATION
18 00840420163301 SB017055 SB017055 HWC Screw, fixation, bone 2 SALVATION
19 00840420163295 SB017050 SB017050 HWC Screw, fixation, bone 2 SALVATION
20 00840420197535 03-5010 03-5010 RX-FIX Mini Rail System HWR DRIVER, PROSTHESIS 1 NA
21 00840420197528 03-5009 03-5009 LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 NA
22 00840420197511 03-5007 03-5007 LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 NA
23 00840420197504 03-5005 03-5005 LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 NA
24 00840420197498 03-5004 03-5004 T-Tool for Rx-Fix LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 NA
25 00840420197481 03-5002 03-5002 LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 NA
26 00840420197474 03-5000 03-5000 LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 NA
27 00840420198808 4940125 KWI PROSTHESIS, ELBOW, HEMI-, RADIAL, POLYMER 2 NA
28 00840420198792 4940115 KWI PROSTHESIS, ELBOW, HEMI-, RADIAL, POLYMER 2 NA
29 00840420198785 4940103 KWI PROSTHESIS, ELBOW, HEMI-, RADIAL, POLYMER 2 NA
30 00840420198778 4940102 KWI PROSTHESIS, ELBOW, HEMI-, RADIAL, POLYMER 2 NA
31 00840420198761 4940101 KWI PROSTHESIS, ELBOW, HEMI-, RADIAL, POLYMER 2 NA
32 00840420197566 03-5015 03-5015 LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 NA
33 00840420199522 8661000 8661000 Trapezium Sizing Set HWT Template 1 TIE-IN
34 00840420197559 03-5013 03-5013 LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 NA
35 00840420163417 SB170110 SB170110 HWC Screw, fixation, bone 2 SALVATION
36 00840420199720 18770140 18770140 Pin Puller LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 NA
37 00840420195425 FFHSIZER FFHSIZER Staple Sizer HWT TEMPLATE 1 FUSEFORCE™
38 00840420194848 SMN10011 SMN10011 Step Drill HTW BIT, DRILL 1 SALVATION
39 00840420194831 SMN10010 SMN10010 Drill HTW BIT, DRILL 1 SALVATION
40 00840420194824 SMN10009 SMN10009 Quick Connector Inserter MDM INSTRUMENT, MANUAL, SURGICAL, GENERAL USE 1 SALVATION
41 00840420194817 SMN10008 SMN10008 Implant Holder Assembly MDM INSTRUMENT, MANUAL, SURGICAL, GENERAL USE 1 SALVATION
42 00840420194800 SMN10007 SMN10007 Targeting Guide Assembly FZX Guide, surgical, instrument 1 SALVATION
43 00840420194657 60006024 60006024 Dome Impaction Block HWA IMPACTOR 1 INVISION
44 00840420194534 IB220705 IB220705 HSN PROSTHESIS, ANKLE, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER 2 INVISION
45 00840420194527 IB220704 IB220704 HSN PROSTHESIS, ANKLE, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER 2 INVISION
46 00840420194510 IB220703 IB220703 HSN PROSTHESIS, ANKLE, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER 2 INVISION
47 00840420194503 IB220702 IB220702 HSN PROSTHESIS, ANKLE, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER 2 INVISION
48 00840420194497 IB220701 IB220701 HSN PROSTHESIS, ANKLE, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER 2 INVISION
49 00840420194435 60011150 60011150 Talar Plate Trial HSN PROSTHESIS, ANKLE, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER 2 INVISION
50 00840420194428 60011140 60011140 Talar Plate Trial HWT TEMPLATE 1 INVISION
Other products with the same Product Code "KWD"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 10381780279471 2031004 2031004 K2™ Hemi Toe Implant System TOE PLATE K2™ Hemi Toe Implant System INTEGRA LIFESCIENCES CORPORATION
2 10381780257240 HEMISET K2™ Hemi Instrument Set (20-6000) K2™ ASCENSION ORTHOPEDICS, INC.
3 10381780237150 PIS89000 The Movement Great Toe proximal phalanx implant sizer allows for clear visualiza The Movement Great Toe proximal phalanx implant sizer allows for clear visualization of the implant size. Movement® ASCENSION ORTHOPEDICS, INC.
4 10381780237143 MIS89000 The Movement Great Toe metatarsal sizer allows for clear visualization of the im The Movement Great Toe metatarsal sizer allows for clear visualization of the implant size. Movement® ASCENSION ORTHOPEDICS, INC.
5 10381780236948 TRL89040PPH The Proximal Phalanx Hemi Trial is used to evaluate the size and fit of the implant. Movement® ASCENSION ORTHOPEDICS, INC.
6 10381780236931 TRL89040MT The Metatarsal Trial is used to evaluate the size and fit of the implant. Movement® ASCENSION ORTHOPEDICS, INC.
7 10381780236917 TRL89030PPH The Proximal Phalanx Hemi Trial is used to evaluate the size and fit of the implant. Movement® ASCENSION ORTHOPEDICS, INC.
8 10381780236900 TRL89030MT The Metatarsal Trial is used to evaluate the size and fit of the implant. Movement® ASCENSION ORTHOPEDICS, INC.
9 10381780236887 TRL89020PPH The Proximal Phalanx Hemi Trial is used to evaluate the size and fit of the implant. Movement® ASCENSION ORTHOPEDICS, INC.
10 10381780236870 TRL89020MT The Metatarsal Trial is used to evaluate the size and fit of the implant. Movement® ASCENSION ORTHOPEDICS, INC.
11 10381780236856 TRL89010PPH The Proximal Phalanx Hemi Trial is used to evaluate the size and fit of the implant. Movement® ASCENSION ORTHOPEDICS, INC.
12 10381780236849 TRL89010MT The Metatarsal Trial is used to evaluate the size and fit of the implant. Movement® ASCENSION ORTHOPEDICS, INC.
13 10381780234999 MOVEMNTINSTP The Movement Great Toe System is used for hemi- and total-arthroplasty procedure The Movement Great Toe System is used for hemi- and total-arthroplasty procedures. The hemi arthroplasty is intended for resurfacing of the 1st metatarsal head or the base of the proximal phalanx. The total arthroplasty is intended for resurfacing of the base of the 1st metatarso-phalangeal joint. This set includes metatarsal, proximal phalanx hemi, and proximal phalanx total trials to evaluate the size and fit of the appropriate implant. Instruments are also included to assist with the trials. Movement® ASCENSION ORTHOPEDICS, INC.
14 10381780116479 MGT89040PPH MGT89040PPH The Integra Movement Great Toe System phalangeal component is designed for resur The Integra Movement Great Toe System phalangeal component is designed for resurfacing the base of the proximal phalanx. The component is an anatomically designed, monolithic device. The device is made from cobalt chromium alloy with a commerically pure titanium plasma spray. The phalangeal component is intended as hemi-arthroplasty at the surface and is press-fit. Integra® MOVEMENT® Great Toe System ASCENSION ORTHOPEDICS, INC.
15 10381780116462 MGT89040MT MGT89040MT The Integra Movement Great Toe System metatarsal component is designed for resur The Integra Movement Great Toe System metatarsal component is designed for resurfacing the 1st metatarsal head. The component is an anatomically designed, monolithic device.The device is made from cobalt chromium alloy with a commercially pure titanium plasma spray. The metatarsal is intended as hemi-arthroplasty at the surface and is a press-fit. Integra® MOVEMENT® Great Toe System ASCENSION ORTHOPEDICS, INC.
16 10381780116455 MGT89030PPH MGT89030PPH The Integra Movement Great Toe System phalangeal component is designed for resur The Integra Movement Great Toe System phalangeal component is designed for resurfacing the base of the proximal phalanx. The component is an anatomically designed, monolithic device. The device is made from cobalt chromium alloy with a commerically pure titanium plasma spray. The phalangeal component is intended as hemi-arthroplasty at the surface and is press-fit. Integra® MOVEMENT® Great Toe System ASCENSION ORTHOPEDICS, INC.
17 10381780116448 MGT89030MT MGT89030MT The Integra Movement Great Toe System metatarsal component is designed for resur The Integra Movement Great Toe System metatarsal component is designed for resurfacing the 1st metatarsal head. The component is an anatomically designed, monolithic device.The device is made from cobalt chromium alloy with a commercially pure titanium plasma spray. The metatarsal is intended as hemi-arthroplasty at the surface and is a press-fit. Integra® MOVEMENT® Great Toe System ASCENSION ORTHOPEDICS, INC.
18 10381780116431 MGT89020PPH MGT89020PPH The Integra Movement Great Toe System phalangeal component is designed for resur The Integra Movement Great Toe System phalangeal component is designed for resurfacing the base of the proximal phalanx. The component is an anatomically designed, monolithic device. The device is made from cobalt chromium alloy with a commerically pure titanium plasma spray. The phalangeal component is intended as hemi-arthroplasty at the surface and is press-fit. Integra® MOVEMENT® Great Toe System ASCENSION ORTHOPEDICS, INC.
19 10381780116424 MGT89020MT MGT89020MT The Integra Movement Great Toe System metatarsal component is designed for resur The Integra Movement Great Toe System metatarsal component is designed for resurfacing the 1st metatarsal head. The component is an anatomically designed, monolithic device.The device is made from cobalt chromium alloy with a commercially pure titanium plasma spray. The metatarsal is intended as hemi-arthroplasty at the surface and is a press-fit. Integra® MOVEMENT® Great Toe System ASCENSION ORTHOPEDICS, INC.
20 10381780116417 MGT89010PPH MGT89010PPH The Integra Movement Great Toe System phalangeal component is designed for resur The Integra Movement Great Toe System phalangeal component is designed for resurfacing the base of the proximal phalanx. The component is an anatomically designed, monolithic device. The device is made from cobalt chromium alloy with a commerically pure titanium plasma spray. The phalangeal component is intended as hemi-arthroplasty at the surface and is press-fit. Integra® MOVEMENT® Great Toe System ASCENSION ORTHOPEDICS, INC.
21 10381780116400 MGT89010MT MGT89010MT The Integra Movement Great Toe System metatarsal component is designed for resur The Integra Movement Great Toe System metatarsal component is designed for resurfacing the 1st metatarsal head. The component is an anatomically designed, monolithic device.The device is made from cobalt chromium alloy with a commercially pure titanium plasma spray. The metatarsal is intended as hemi-arthroplasty at the surface and is a press-fit. Integra® MOVEMENT® Great Toe System ASCENSION ORTHOPEDICS, INC.
22 10381780116394 HM2300 HM2300 The Integra® BioMotion® Cannulated Hemi implant is used with the Integra® BioM The Integra® BioMotion® Cannulated Hemi implant is used with the Integra® BioMotion® Cannulated Hemi System as a partial joint replacement for the first metatarsophalangeal joint (MPJ). The Cannulated Implants are made from Titanium Alloy (ASTM F-136). Integra® BioMotion® Cannulated Hemi System ASCENSION ORTHOPEDICS, INC.
23 10381780116387 HM2100 HM2100 The Integra® BioMotion® Cannulated Hemi implant is used with the Integra® BioM The Integra® BioMotion® Cannulated Hemi implant is used with the Integra® BioMotion® Cannulated Hemi System as a partial joint replacement for the first metatarsophalangeal joint (MPJ). The Cannulated Implants are made from Titanium Alloy (ASTM F-136). Integra® BioMotion® Cannulated Hemi System ASCENSION ORTHOPEDICS, INC.
24 10381780116370 HM1900 HM1900 The Integra® BioMotion® Cannulated Hemi implant is used with the Integra® BioM The Integra® BioMotion® Cannulated Hemi implant is used with the Integra® BioMotion® Cannulated Hemi System as a partial joint replacement for the first metatarsophalangeal joint (MPJ). The Cannulated Implants are made from Titanium Alloy (ASTM F-136). Integra® BioMotion® Cannulated Hemi System ASCENSION ORTHOPEDICS, INC.
25 10381780116363 HM1700 HM1700 The Integra® BioMotion® Cannulated Hemi implant is used with the Integra® BioM The Integra® BioMotion® Cannulated Hemi implant is used with the Integra® BioMotion® Cannulated Hemi System as a partial joint replacement for the first metatarsophalangeal joint (MPJ). The Cannulated Implants are made from Titanium Alloy (ASTM F-136). Integra® BioMotion® Cannulated Hemi System ASCENSION ORTHOPEDICS, INC.
26 10381780116356 HM1500 HM1500 The Integra® BioMotion® Cannulated Hemi implant is used with the Integra® BioM The Integra® BioMotion® Cannulated Hemi implant is used with the Integra® BioMotion® Cannulated Hemi System as a partial joint replacement for the first metatarsophalangeal joint (MPJ). The Cannulated Implants are made from Titanium Alloy (ASTM F-136). Integra® BioMotion® Cannulated Hemi System ASCENSION ORTHOPEDICS, INC.
27 10381780074274 BIOMOTIONIMP BIOMOTIONIMP The Integra BioMotion Cannulated Hemi System is a partial joint replacement syst The Integra BioMotion Cannulated Hemi System is a partial joint replacement system for the first metatarsophalangeal joint (MPJ). Implants are available in sizes ranging from 15mm to 23mm. The system includes instruments to facilitate the placement of the implants. All implants are made from Titanium Alloy, and instrumentation is made from titanium and stainless steel. The BioMotion hemi implant is indicated for use in the treatment of degenerative arthritis in the first MPJ along with hallux limitus/rigidus, hallux valgus and pain or instability. Integra® BioMotion® Cannulated Hemi System ASCENSION ORTHOPEDICS, INC.
28 10381780065579 201040 201040 The K2 Hemi Toe implant is intended for cement fixation by means of a stem, whic The K2 Hemi Toe implant is intended for cement fixation by means of a stem, which is inserted into the medullary canal of the phalanx. It is indicated for use in patients with osteoarthritis of the first metatarsophalangeal joint, trauma involving the first metatarsophalangeal joint, hallux rigidus with degenerative joint disease or arthritis. K2™ Hemi Toe Implant System INTEGRA LIFESCIENCES CORPORATION
29 10381780065562 201030 201030 The K2 Hemi Toe implant is intended for cement fixation by means of a stem, whic The K2 Hemi Toe implant is intended for cement fixation by means of a stem, which is inserted into the medullary canal of the phalanx. It is indicated for use in patients with osteoarthritis of the first metatarsophalangeal joint, trauma involving the first metatarsophalangeal joint, hallux rigidus with degenerative joint disease or arthritis. K2™ Hemi Toe Implant System ASCENSION ORTHOPEDICS, INC.
30 10381780065555 201020 201020 The K2 Hemi Toe implant is intended for cement fixation by means of a stem, whic The K2 Hemi Toe implant is intended for cement fixation by means of a stem, which is inserted into the medullary canal of the phalanx. It is indicated for use in patients with osteoarthritis of the first metatarsophalangeal joint, trauma involving the first metatarsophalangeal joint, hallux rigidus with degenerative joint disease or arthritis. K2™ Hemi Toe Implant System INTEGRA LIFESCIENCES CORPORATION
31 10381780065548 201010 201010 The K2 Hemi Toe implant is intended for cement fixation by means of a stem, whic The K2 Hemi Toe implant is intended for cement fixation by means of a stem, which is inserted into the medullary canal of the phalanx. It is indicated for use in patients with osteoarthritis of the first metatarsophalangeal joint, trauma involving the first metatarsophalangeal joint, hallux rigidus with degenerative joint disease or arthritis. K2™ Hemi Toe Implant System INTEGRA LIFESCIENCES CORPORATION
32 M5289P15S180W0 9P15-S180-W 9P15-S180-W Fixation Component , DF-P HemiCAPDF-P® ARTHROSURFACE INCORPORATED
33 M5289P15PB02W0 9P15-PB02-W 9P15-PB02-W Modular Insert, 1.5mm Offset-02(4.6mm Thick) HemiCAPDF-P® ARTHROSURFACE INCORPORATED
34 M5289P15PB01W0 9P15-PB01-W 9P15-PB01-W Modular Insert, 1.5mm Offset-01(3.6mm Thick) HemiCAPDF-P® ARTHROSURFACE INCORPORATED
35 M5289P15PA02W0 9P15-PA02-W 9P15-PA02-W Modular Insert, 1.5mm Offset-02(4.6mm Thick) HemiCAPDF-P® ARTHROSURFACE INCORPORATED
36 M5289M522545W0 9M52-2545-W 9M52-2545-W 15mm Articular Comp,TOE2, 2.5mm x 4.5mm CE HemiCAPDF® ARTHROSURFACE INCORPORATED
37 M5289M522545A0 9M52-2545-A 9M52-2545-A 15mm Articular Comp,TOE2, 2.5mm x 4.5mm HemiCAPDF® ARTHROSURFACE INCORPORATED
38 M5289M522535W0 9M52-2535-W 9M52-2535-W 15mm Articular Comp,TOE2, 2.5mm x 3.5mm MTP CE HemiCAPDF® ARTHROSURFACE INCORPORATED
39 M5289M522535A0 9M52-2535-A 9M52-2535-A 15mm Articular Comp,TOE2, 2.5mm x 3.5mm MTP HemiCAPDF® ARTHROSURFACE INCORPORATED
40 M5289M521545W0 9M52-1545-W 9M52-1545-W 15mm Articular Comp,TOE2, 1.5mm x 4.5mm MTP CE HemiCAPDF® ARTHROSURFACE INCORPORATED
41 M5289M521545A0 9M52-1545-A 9M52-1545-A 15mm Articular Comp,TOE2, 1.5mm x 4.5mm MTP HemiCAPDF® ARTHROSURFACE INCORPORATED
42 M5289M521535W0 9M52-1535-W 9M52-1535-W 15mm Articular Comp,TOE2, 1.5mm x 3.5mm MTP CE HemiCAPDF® ARTHROSURFACE INCORPORATED
43 M5289M521535A0 9M52-1535-A 9M52-1535-A 15mm Articular Comp,TOE2, 1.5mm x 3.5mm MTP HemiCAPDF® ARTHROSURFACE INCORPORATED
44 M5289L15S080A0 9L15-S080-A 9L15-S080-A Taper Post, MTP, Phalangeal BaseCap ARTHROSURFACE INCORPORATED
45 M5289L150040A0 9L15-0040-A 9L15-0040-A Articular Component, Curvature #40 BaseCap ARTHROSURFACE INCORPORATED
46 M5289L150030A0 9L15-0030-A 9L15-0030-A Articular Component, Curvature #30 BaseCap ARTHROSURFACE INCORPORATED
47 M5289L150020A0 9L15-0020-A 9L15-0020-A Articular Component, Curvature #20 BaseCap ARTHROSURFACE INCORPORATED
48 M5289L150010A0 9L15-0010-A 9L15-0010-A Articular Component, Curvature #10 BaseCap ARTHROSURFACE INCORPORATED
49 M5289F15PA01W0 9P15-PA01-W 9P15-PA01-W Modular Insert, 1.5mm Offset-01(3.6mm Thick) HemiCAPDF-P® ARTHROSURFACE INCORPORATED
50 M5289CRSD200A0 9CRS-D200-A 9CRS-D200-A Taper Post, BOSS, 10.0mm (18.5mm LG) BOSS Toe Fixation System ARTHROSURFACE INCORPORATED