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Medical Device Technologies, Inc.
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INTER V BRAND V-MARK BREAST BIOPSY SITE MARKER WITH TITANIUM ANCHOR is an FDA 510(k)-cleared medical device (K051421) manufactured by Medical Device Technologies, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 29, 2005. Regulation: 8.