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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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).
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).
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).
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).
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).
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.
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.
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.
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.
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.