MODIFIED RETRIEVER (MODIFIED, LINE EXTENSION), MODELS 90152, 90153

MODIFIED RETRIEVER (MODIFIED, LINE EXTENSION), MODELS 90152, 90153 is an FDA 510(k)-cleared medical device (K093610) manufactured by Concentric Medical, 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 16, 2011. Regulation: 8.