Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Sintea Plastek, LLC

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K112611 SINTEA PLUSTEK PLS MULTI-AXIAL SCREWSMNI2012-04-25 View
510(k) K101886 DSC/ALF SPINAL SYSTEMMQP2011-07-21 View
↑