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Sintea Plustek, LLC

3 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
PLS (POSTERIOR LUMBAR SYSTEM) (K140787)Sintea Plustek, LLC2014-05-30
SPIDER SYSTEM KOLIBRI CEMENT NEEDLE (K130402)Sintea Plustek, LLC2013-04-01
SINTEA PLUSTEK ANTERIOR CERVICAL PLATE SYSTEM (K112861)Sintea Plustek, LLC2012-02-24

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Every clearance here is in the API, with alerts when new ones post.