LUX-Dx Insertable Cardiac Monitor Remote Programming and Performance Study

Inclusion Criteria: * Patient is indicated to be implanted with the LUX-Dx ICM for one of the following reasons (grouped in three "Reason for Monitoring" subgroups): 1) Cryptogenic stroke, 2) Syncope, 3) AF management, Post-AF ablation, or Suspected AF * Patient is willing to enroll and be monitored in LATITUDE Clarity. * Patient is willing and able to be followed remotely via the ICM patient mobile app. * Patient is willing and capable of providing informed consent (which is not to include the use of a legally authorized representative (LAR) for documentation of informed consent) and agrees to participate in all protocol required activities. * Patient is age 18 years or above, or of legal age to give informed consent specific to state and national law. The following inclusion criterion is applicable for patients participating in the Holter study: • Patient can tolerate the adhesive used in the Holter monitoring for an extended period of time. Exclusion Criteria: * Patient is indicated for implantation of, or is currently implanted with an active implantable cardiac device (e.g., LVAD, ICD, CRT D, PPM\*). * Patient cannot tolerate a subcutaneous, chronically-inserted device due to medical condition. * Patient has a documented life expectancy of less than 12 months (per investigator's discretion). * Patient is known to be pregnant at the time of study enrollment (method of assessment upon investigator's discretion). * Patient is currently enrolled in another clinical stud…