FDA 510(k) Applications Submitted by RICHARD A OVERTON

FDA 510(k) Number Submission Date Device Name Applicant
K072878 10/09/2007 MODIFICATION TO: LOCATOR IMPLANT ANCHOR ZEST ANCHORS, INC.
K083324 11/12/2008 LOCATOR IMPLANT ANCHOR ATTACHMENT SYSTEM ZEST ANCHORS, INC.


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