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Acorn Group, Inc.

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K914362 TOP CERVICAL SPINE PLATES & TITANIUM BONE SCREWSKWQ1992-04-29 View
510(k) K912905 LARYNGOSCOPECCW1991-09-30 View
510(k) K904126 VISIRASERGEX1990-10-30 View
510(k) K900430 IRRIGATION AND SUCTION APPARATUSJCX1990-06-05 View
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