The NexStent® Carotid Stent System: A Post Market Approval Evaluation Study In Conjunction With the FilterWire EZ™ Embolic Protection System
The NexStent® Carotid Stent System: A Post Market Approval Evaluation Study In Conjunction With the FilterWire EZ™ Embolic Protection System
The primary objective of the SONOMA Registry is to confirm the safety of the NexStent® Carotid Stent System and FilterWire EZ™ Embolic Protection System in routine clinical practice and to identify rare or unanticipated device-related events that might occur.
The SONOMA Registry will enroll approximately 300 subjects at a maximum at 78 study centers.
Inclusion Criteria:
Exclusion Criteria:
Miami, Florida 33176, United States
Kingsport, Tennessee 37660, United States