This study is designed to collect data on the complication rates and procedural success of using a transradial access approach to treat peripheral lesions in the lower extremities of a real world population.

Inclusion Criteria:

• Rutherford Category 2-5
• Subject scheduled for a transradial intervention to treat a lesion in the lower extremities.
• Willing to sign consent and agree to follow-up requirements.

Exclusion Criteria:

• Previous failed transradial access attempt
• Presence of or planned dialysis fistula.
• Planned amputation
• Previous or planned transradial access intervention +/- 30 days
• Radial artery diameter <2.5mm
• No palpable radial artery
• Established vasospastic disease
• Known allergy to contrast that cannot be managed
• Pregnant or lactating
• Mentally incompetent or a prisoner
• Currently participating in a clinical study that has not completed it's primary endpoint

Subjects planned to undergo treatment of a lower extremity lesion via transradial artery access.