Life Spine lateral fixation device gains FDA clearance

The FDA provided Life Spine 510(k) clearance for its Prolift lateral fixated system on April 21.

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Three things to know:

1. The Prolift expandable system features fixation and cam locks that assist the surgeon with final locking.

2. Surgeons can post pack the device in-situ through the inserter.

3. The Prolift system comes in a variety of footprints and combines with Life Spine’s Sentry lateral plate to facilitate lateral spine procedures.

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