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Ankle Replacement System Boone NC

A total ankle replacement system in Boone that may preserve some range of motion in arthritic or deformed ankles has been approved by the U.S. Food and Drug Administration. The Scandinavian Total Ankle Replacement (STAR) system is the first of its type and uses bearings that move across a surface of flexible plastic (polyethylene).

Appalachian - New River Veterinary Associates
(828) 264-5621
218 Wilson Dr
Boone, NC

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Juan Carlos De Virgiliis
(828) 262-3733
381 Deerfield Rd
Boone, NC
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(828) 262-3733
381 Deerfield Road
Boone, NC
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(828) 264-0550
950 State Farm Rd
Boone, NC
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(828) 262-0060
136 Furman Rd
Boone, NC
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Dean Steven Cohen
(828) 262-4200
336 Deerfield Rd
Boone, NC
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Robert C Snyder
(828) 268-0064
237 Longvue Dr
Boone, NC
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Health & Wellness Initiatives
(828) 260-6297
409 Russelton Road
Boone, NC
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Charlie L Sykes
(828) 264-6362
108 Doctors Dr
Boone, NC
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(828) 264-6362
108 Doctors Dr
Boone, NC
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Ankle Replacement System

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THURSDAY, May 28 (HealthDay News) -- A total ankle replacement system that may preserve some range of motion in arthritic or deformed ankles has been approved by the U.S. Food and Drug Administration.

The Scandinavian Total Ankle Replacement (STAR) system is the first of its type and uses bearings that move across a surface of flexible plastic (polyethylene).

Total ankle replacement is considered when arthritis or injury has destroyed the cartilage that cushions the ankle bone.

The new device offers an alternative to fusion surgery, in which the shin bone is cemented to the talus bone in the ankle. While fusion surgery stabilizes the ankle, it significantly decreases a patient's ability to move their foot up and down.

"This device offers another treatment alternative to fusion surgery, and more closely imitates the function of a natural ankle. For the first time in the United States, a patient may retain some ankle mobility with this non-constrained, mobile-bearing device," Dr. Daniel G. Schultz, director of the FDA's Center for Devices and Radiological Health, said in an agency news release.

The FDA's approval of the STAR system is based on a two-year study of 224 patients that found the device had similar rates of adverse events, surgical interventions and major complications as fusion surgery. As a condition of the approval, Small Bone Innovations of Pennsylvania will evaluate the safety and effectiveness of its device over the next eight years.

Other options to fusion surgery include several fixed-bearing devices in which the articulating surface is molded, locked or attached to one of its metallic components.

More information

The MedlinePlus Medical Encyclopedia has more about ankle replacement.

SOURCE: U.S. Food and Drug Administration, news release, May 27, 2009

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