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Sintea Plustek, LLC

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K130402 SPIDER SYSTEM KOLIBRI CEMENT NEEDLENDN2013-04-01 View
510(k) K112861 SINTEA PLUSTEK ANTERIOR CERVICAL PLATE SYSTEMKWQ2012-02-24 View
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