TITANIUM PERCUTANEOUS GREENFIELD VENA CAVE FILTER

TITANIUM PERCUTANEOUS GREENFIELD VENA CAVE FILTER is an FDA 510(k)-cleared medical device (K870729) manufactured by Medi-Tech, 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 April 8, 1987. Regulation: 8.