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.

Nextremity Solutions, LLC

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K122031 NEXTRA TI HAMMERTOE CORRECTION SYSTEMHWC2012-10-09 View
510(k) K110445 FLEXFUSION (TM) FIXATION IMPLANTHWC2011-03-17 View
↑