Post-Market Registry
Patient or legally authorized representative (LAR) provides authorization and/or consent per institution and geographical requirements.
Participant is treated or intended to be treated with a commercially available Medtronic Neurovascular device* during treatment for acute ischemic stroke.
Participant is 18 years of age or older.
Participant who may be unable to complete follow-up within the registry.
Participant of child-bearing potential who is known to be pregnant or is breastfeeding or wishes to become pregnant during participation in the study.
Participant is currently enrolled in, or plans to enroll in, any concurrent drug/device study that may confound the study results based on Principal Investigator's discretion.