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.

Precimed, Inc.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K050754 PRECIMED CANNULATED SCREW SYSTEMHWC2005-05-18 View
510(k) K023851 PRECIMED HIP SCREW SYSTEMKTT2003-01-28 View
↑