Other products from "TORNIER, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00846832063253 FHS-010-25-40L HWC Screw, fixation, bone 2 ForeFoot STP
2 00846832066421 DWK403LA25S KWS PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED 2 Aequalis™ PerFORM+
3 00846832064304 FHS-076-31W-12 FHS-076-31W-12 HWC Screw, fixation, bone 2 ForeFoot STP
4 00846832064298 MXM-068C LXH Orthopedic Manual Surgical Instrument 1 ForeFoot STP
5 00846832063802 FHS-010-30F-44 HWC Screw, fixation, bone 2 ForeFoot STP
6 00846832063796 FHS-010-30F-42 HWC Screw, fixation, bone 2 ForeFoot STP
7 00846832063765 FHS-010-30F-36 HWC Screw, fixation, bone 2 ForeFoot STP
8 00846832063703 FHS-010-30F-24 HWC Screw, fixation, bone 2 ForeFoot STP
9 00846832063185 FHS-010-25-26L FHS-010-25-26L HWC Screw, fixation, bone 2 ForeFoot STP
10 00846832063116 FHS-010-25-12L HWC Screw, fixation, bone 2 ForeFoot STP
11 00846832063031 FHS-010-20F-18 HWC Screw, fixation, bone 2 ForeFoot STP
12 00846832085842 MWJ10461 MWJ10461 PHX,KWS shoulder prosthesis, reverse configuration,PROSTHESIS, SHOULDER, SEMI-CONSTRAINE shoulder prosthesis, reverse configuration,PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED 2 TORNIER PERFORM™ REVERSED
13 00846832085798 DWJ1017702 DWJ1017702 KWS,PHX PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED,shoulder prosthes PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED,shoulder prosthesis, reverse configuration 2 TORNIER PERFORM™ REVERSED
14 00846832073641 SPS350 SPS350 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
15 00846832073634 SPS348 SPS348 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
16 00846832073627 SPS346 SPS346 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
17 00846832073610 SPS344 SPS344 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
18 00846832073597 SPS340 SPS340 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
19 00846832073580 SPS338 SPS338 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
20 00846832073573 SPS336 SPS336 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
21 00846832073566 SPS334 SPS334 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
22 00846832073559 SPS332 SPS332 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
23 00846832073542 SPS330 SPS330 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
24 00846832073535 SPS328 SPS328 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
25 00846832073511 SPS324 SPS324 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
26 00846832073504 SPS322 SPS322 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
27 00846832073481 SPS318 SPS318 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
28 00846832073474 SPS316 SPS316 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
29 00846832073344 SPS232 SPS232 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
30 00846832073337 SPS230 SPS230 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
31 00846832073320 SPS228 SPS228 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
32 00846832073313 SPS226 SPS226 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
33 00846832073306 SPS224 SPS224 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
34 00846832073283 SPS220 SPS220 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
35 00846832073276 SPS218 SPS218 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
36 00846832073269 SPS216 SPS216 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
37 00846832073252 SPS156 SPS156 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
38 00846832073245 SPS154 SPS154 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
39 00846832073238 SPS152 SPS152 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
40 00846832073221 SPS150 SPS150 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
41 00846832073214 SPS148 SPS148 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
42 00846832073191 SPS144 SPS144 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
43 00846832073184 SPS142 SPS142 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
44 00846832073177 SPS140 SPS140 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
45 00846832073153 SPS136 SPS136 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
46 00846832073146 SPS134 SPS134 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
47 00846832073122 SPS130 SPS130 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
48 00846832073115 SPS128 SPS128 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
49 00846832073108 SPS126 SPS126 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
50 00846832073092 SPS124 SPS124 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
Other products with the same Product Codes "KYI, 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 10381780236580 TRL44340M TRL-443-40M The NuGrip Trial is used to evaluate the size and fit of the implant. Integra® NuGrip® ASCENSION ORTHOPEDICS, INC.
14 10381780236573 TRL44340L TRL-443-40L The NuGrip Trial is used to evaluate the size and fit of the implant. Integra® NuGrip® ASCENSION ORTHOPEDICS, INC.
15 10381780236566 TRL44330S TRL-443-30S The NuGrip Trial is used to evaluate the size and fit of the implant. Integra® NuGrip® ASCENSION ORTHOPEDICS, INC.
16 10381780236559 TRL44330M TRL-443-30M The NuGrip Trial is used to evaluate the size and fit of the implant. Integra® NuGrip® ASCENSION ORTHOPEDICS, INC.
17 10381780236542 TRL44330L TRL-443-30L The NuGrip Trial is used to evaluate the size and fit of the implant. Integra® NuGrip® ASCENSION ORTHOPEDICS, INC.
18 10381780236535 TRL44320S TRL-443-20S The NuGrip Trial is used to evaluate the size and fit of the implant. Integra® NuGrip® ASCENSION ORTHOPEDICS, INC.
19 10381780236528 TRL44320M TRL-443-20M The NuGrip Trial is used to evaluate the size and fit of the implant. Integra® NuGrip® ASCENSION ORTHOPEDICS, INC.
20 10381780236511 TRL44310S TRL-443-10S The NuGrip Trial is used to evaluate the size and fit of the implant. Integra® NuGrip® ASCENSION ORTHOPEDICS, INC.
21 10381780236504 TRL44310M TRL-443-10M The NuGrip Trial is used to evaluate the size and fit of the implant. Integra® NuGrip® ASCENSION ORTHOPEDICS, INC.
22 10381780236498 TRL43550 TRL-435-50 Trial used to evaluate the size and fit of the implant. Integra® PyroSphere® ASCENSION ORTHOPEDICS, INC.
23 10381780236481 TRL43540 TRL-435-40 Trial used to evaluate the size and fit of the implant. Integra® PyroSphere® ASCENSION ORTHOPEDICS, INC.
24 10381780236474 TRL43530 TRL-435-30 Trial used to evaluate the size and fit of the implant. Integra® PyroSphere® ASCENSION ORTHOPEDICS, INC.
25 10381780236467 TRL43520 TRL-435-20 Trial used to evaluate the size and fit of the implant. Integra® PyroSphere® ASCENSION ORTHOPEDICS, INC.
26 10381780236450 TRL43510 TRL-435-10 Trial used to evaluate the size and fit of the implant. Integra® PyroSphere® ASCENSION ORTHOPEDICS, INC.
27 10381780235033 PYROHEMIINSP The Ascension® PyroHemiSphereTM is intended to replace the proximal end of the f The Ascension® PyroHemiSphereTM is intended to replace the proximal end of the first metacarpal in cases of rheumatoid arthritis, traumatic arthritis, osteoarthritis or post fracture deformation or bone loss which present as either a painful, unstable thumb, or a thumb with limited range of motion. PyroHemiSphereTM ASCENSION ORTHOPEDICS, INC.
28 10381780235019 NUGRIPINSTP The Integra NuGrip system is intended to replace the proximal end of the first m The Integra NuGrip system is intended to replace the proximal end of the first metacarpal in cases of rheumatoid arthritis, traumatic arthritis, osteo-arthritis or post fracture deformation of bone loss which present as either a painful, unstable thumb, or a thumb with limited range of motion. This set includes trials to evaluate the size and fit of the implant. Instruments are included for assistance. Integra® NuGrip® ASCENSION ORTHOPEDICS, INC.
29 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.
30 10381780120131 NUG44340M NUG-443-40M The Ascension® NuGrip® is an uncemented, one-component prosthesis for the basal The Ascension® NuGrip® is an uncemented, one-component prosthesis for the basal thumb joint. It has a proximal head that articulates against the trapezium, a planar collar that provides for a simple planar bone resection, and an anatomic shaped stem that is press fit into the canal of the first metacarpal following resection of the base. It is fabricated from a thick pyrocarbon layer encasing a graphite core that is impregnated with one-atomic percent tungsten so it is radiopaque. The Ascension® NuGrip® is intended to replace the proximal end of the first metacarpal in cases of rheumatoid arthritis, traumatic arthritis, osteoarthritis or post fracture deformation or bone loss which present as either a painful, unstable thumb, or a thumb with limited range of motion. Ascension® NuGrip® ASCENSION ORTHOPEDICS, INC.
31 10381780120124 NUG44340L NUG-443-40L The Ascension® NuGrip® is an uncemented, one-component prosthesis for the basal The Ascension® NuGrip® is an uncemented, one-component prosthesis for the basal thumb joint. It has a proximal head that articulates against the trapezium, a planar collar that provides for a simple planar bone resection, and an anatomic shaped stem that is press fit into the canal of the first metacarpal following resection of the base. It is fabricated from a thick pyrocarbon layer encasing a graphite core that is impregnated with one-atomic percent tungsten so it is radiopaque. The Ascension® NuGrip® is intended to replace the proximal end of the first metacarpal in cases of rheumatoid arthritis, traumatic arthritis, osteoarthritis or post fracture deformation or bone loss which present as either a painful, unstable thumb, or a thumb with limited range of motion. Ascension® NuGrip® ASCENSION ORTHOPEDICS, INC.
32 10381780120117 NUG44330S NUG-443-30S The Ascension® NuGrip® is an uncemented, one-component prosthesis for the basal The Ascension® NuGrip® is an uncemented, one-component prosthesis for the basal thumb joint. It has a proximal head that articulates against the trapezium, a planar collar that provides for a simple planar bone resection, and an anatomic shaped stem that is press fit into the canal of the first metacarpal following resection of the base. It is fabricated from a thick pyrocarbon layer encasing a graphite core that is impregnated with one-atomic percent tungsten so it is radiopaque. The Ascension® NuGrip® is intended to replace the proximal end of the first metacarpal in cases of rheumatoid arthritis, traumatic arthritis, osteoarthritis or post fracture deformation or bone loss which present as either a painful, unstable thumb, or a thumb with limited range of motion. Ascension® NuGrip® ASCENSION ORTHOPEDICS, INC.
33 10381780120100 NUG44330M NUG-443-30M The Ascension® NuGrip® is an uncemented, one-component prosthesis for the basal The Ascension® NuGrip® is an uncemented, one-component prosthesis for the basal thumb joint. It has a proximal head that articulates against the trapezium, a planar collar that provides for a simple planar bone resection, and an anatomic shaped stem that is press fit into the canal of the first metacarpal following resection of the base. It is fabricated from a thick pyrocarbon layer encasing a graphite core that is impregnated with one-atomic percent tungsten so it is radiopaque. The Ascension® NuGrip® is intended to replace the proximal end of the first metacarpal in cases of rheumatoid arthritis, traumatic arthritis, osteoarthritis or post fracture deformation or bone loss which present as either a painful, unstable thumb, or a thumb with limited range of motion. Ascension® NuGrip® ASCENSION ORTHOPEDICS, INC.
34 10381780120094 NUG44330L NUG-443-30L The Ascension® NuGrip® is an uncemented, one-component prosthesis for the basal The Ascension® NuGrip® is an uncemented, one-component prosthesis for the basal thumb joint. It has a proximal head that articulates against the trapezium, a planar collar that provides for a simple planar bone resection, and an anatomic shaped stem that is press fit into the canal of the first metacarpal following resection of the base. It is fabricated from a thick pyrocarbon layer encasing a graphite core that is impregnated with one-atomic percent tungsten so it is radiopaque. The Ascension® NuGrip® is intended to replace the proximal end of the first metacarpal in cases of rheumatoid arthritis, traumatic arthritis, osteoarthritis or post fracture deformation or bone loss which present as either a painful, unstable thumb, or a thumb with limited range of motion. Ascension® NuGrip® ASCENSION ORTHOPEDICS, INC.
35 10381780120087 NUG44320S NUG-443-20S The Ascension® NuGrip® is an uncemented, one-component prosthesis for the basal The Ascension® NuGrip® is an uncemented, one-component prosthesis for the basal thumb joint. It has a proximal head that articulates against the trapezium, a planar collar that provides for a simple planar bone resection, and an anatomic shaped stem that is press fit into the canal of the first metacarpal following resection of the base. It is fabricated from a thick pyrocarbon layer encasing a graphite core that is impregnated with one-atomic percent tungsten so it is radiopaque. The Ascension® NuGrip® is intended to replace the proximal end of the first metacarpal in cases of rheumatoid arthritis, traumatic arthritis, osteoarthritis or post fracture deformation or bone loss which present as either a painful, unstable thumb, or a thumb with limited range of motion. Ascension® NuGrip® ASCENSION ORTHOPEDICS, INC.
36 10381780120070 NUG44320M NUG-443-20M The Ascension® NuGrip® is an uncemented, one-component prosthesis for the basal The Ascension® NuGrip® is an uncemented, one-component prosthesis for the basal thumb joint. It has a proximal head that articulates against the trapezium, a planar collar that provides for a simple planar bone resection, and an anatomic shaped stem that is press fit into the canal of the first metacarpal following resection of the base. It is fabricated from a thick pyrocarbon layer encasing a graphite core that is impregnated with one-atomic percent tungsten so it is radiopaque. The Ascension® NuGrip® is intended to replace the proximal end of the first metacarpal in cases of rheumatoid arthritis, traumatic arthritis, osteoarthritis or post fracture deformation or bone loss which present as either a painful, unstable thumb, or a thumb with limited range of motion. Ascension® NuGrip® ASCENSION ORTHOPEDICS, INC.
37 10381780120063 NUG44310S NUG-443-10S The Ascension® NuGrip® is an uncemented, one-component prosthesis for the basal The Ascension® NuGrip® is an uncemented, one-component prosthesis for the basal thumb joint. It has a proximal head that articulates against the trapezium, a planar collar that provides for a simple planar bone resection, and an anatomic shaped stem that is press fit into the canal of the first metacarpal following resection of the base. It is fabricated from a thick pyrocarbon layer encasing a graphite core that is impregnated with one-atomic percent tungsten so it is radiopaque. The Ascension® NuGrip® is intended to replace the proximal end of the first metacarpal in cases of rheumatoid arthritis, traumatic arthritis, osteoarthritis or post fracture deformation or bone loss which present as either a painful, unstable thumb, or a thumb with limited range of motion. Ascension® NuGrip® ASCENSION ORTHOPEDICS, INC.
38 10381780120056 NUG44310M NUG-443-10M The Ascension® NuGrip® is an uncemented, one-component prosthesis for the basal The Ascension® NuGrip® is an uncemented, one-component prosthesis for the basal thumb joint. It has a proximal head that articulates against the trapezium, a planar collar that provides for a simple planar bone resection, and an anatomic shaped stem that is press fit into the canal of the first metacarpal following resection of the base. It is fabricated from a thick pyrocarbon layer encasing a graphite core that is impregnated with one-atomic percent tungsten so it is radiopaque. The Ascension® NuGrip® is intended to replace the proximal end of the first metacarpal in cases of rheumatoid arthritis, traumatic arthritis, osteoarthritis or post fracture deformation or bone loss which present as either a painful, unstable thumb, or a thumb with limited range of motion. Ascension® NuGrip® ASCENSION ORTHOPEDICS, INC.
39 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.
40 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.
41 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.
42 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.
43 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.
44 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.
45 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.
46 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.
47 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.
48 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.
49 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.
50 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.