FDA grants 510(k) clearance for Allevion Medical’s Vantage system

Vantage's intuitive three-step workflow, locate, dilate, decompress, enables physicians to perform procedures with consistency.

Allevion Medical has secured the US Food and Drug Administration (FDA) 510(k) clearance for Vantage, a fully disposable and sterile system intended to simplify and improve minimally invasive spinal decompression procedures.

Vantage allows for targeted treatment through a patented method that combines procedural precision and control.

Its intuitive three-step workflow, locate, dilate, decompress, enables physicians to perform procedures with improved consistency.

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