Registry of Central Sleep Apnea Patients Undergoing remedē System Implant

The goal of this observational study is to collect information on the safety and performance of the remedē System in patients with central sleep apnea who are undergoing the remedē System implant procedure. The main question\[s\] it aims to answer \[is/are\]: What is the incidence of serious adverse events related to the remedē System implant procedure, device, or delivered therapy through 12 months post implant. Participants will complete 2 home sleep apnea tests and be asked about adverse events. All other data collected will be from standard of care visits.