Medtronic Receives Expanded FDA Clearance for Pillar Palatal Implant System

Medtronic has announced it has received expanded FDA clearance for its Pillar Palatal Implant system, according to a news release.

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The system is designed to help reduce snoring severity. It was previously approved for the treatment of snoring and sleep apnea. The new approval allows ENT surgeons to use up to five Pillar implants specifically for snoring, which the company said will help patients with wider mouths and softer palate tissue.

 

“The National Sleep Foundation estimates that nearly 90 million American adults are affected by snoring,” said Janis Saunier, marketing director for the surgical technologies division at Medtronic, in the release. “We’re pleased that we can now offer the Pillar procedure to patients who previously were not candidates.”

 

Medtronic is headquartered in Minneapolis.

 

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