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Norland's X-ray device will assess fracture risk:

This article was originally published in Clinica

Executive Summary

Norland Medical Systems has received 510(k) clearance from the FDA to market a fracture risk assessment feature on its Apollo DXA peripheral bone densitometer. Until recently, doctors could not easily predict which osteoporosis sufferers were at high risk of a bone fracture, but last year the FDA determined that manufacturers of bone density devices could offer a feature which would help. This feature is already available on Norland's pDEXA device.

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