Name: MODIFICATION TO: AGILITY STEERABLE GUIDEWIRES
Brand: Cordis Neurovascular, Inc.
SKU: K010511

MODIFICATION TO: AGILITY STEERABLE GUIDEWIRES is an FDA 510(k)-cleared medical device (K010511) manufactured by Cordis Neurovascular, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 28, 2001. Regulation: 8.

MODIFICATION TO: AGILITY STEERABLE GUIDEWIRES

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