Details.
FDA-approved implantable device therapy for moderate to severe obstructive sleep apnea, intended for patients who cannot tolerate CPAP or have not received consistent benefit from it. The evaluation includes a consultation with a sleep surgeon and a sleep endoscopy to confirm eligibility. The procedure is outpatient surgery performed under general anesthesia, with device implantation through two small incisions. Patients typically go home the same day, recover in about one week, and can begin using the device one month after surgery.