FORCEPS CLIPRACK VENTRICULAR CANNULA SAWS SPATULAS

FORCEPS CLIPRACK VENTRICULAR CANNULA SAWS SPATULAS is an FDA 510(k)-cleared medical device (K874962) manufactured by Solway, Inc.. This device is classified under the Neurology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on February 1, 1988. Regulation: 8.