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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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