
Codman & Shurtleff, Inc.
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VANDERBILT PITUITARY RETRACTOR is an FDA 510(k)-cleared medical device (K761096) manufactured by Codman & Shurtleff, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 29, 1976. Regulation: 8.