Jan 16 (Reuters) - Spineguard Sa ALSGD.PA
* Has received 510(k) clearance from U.S. Food and Drug Administration (FDA) for its new
dynamic surgical guidance integration module to be used in combination with Zavation's spinal
fusion system to make its pedicle screws "Smart"
* Initial US commercialization to begin immediately, will be in combination with Zavation's
pedicle screw system
Source text for Eikon: ID:nBw8yTJZqa
Further company coverage: ALSGD.PA
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