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.

Axiom Worldwide, Inc.

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K060735 DRX9000 TRUE SPINAL DECOMPRESSION SYSTEMITH2006-05-26 View
510(k) K051135 AXIOM NVP8500IPF2005-08-11 View
510(k) K050687 AXIOM EPS8000IPF2005-07-28 View
510(k) K010292 DRX 2000ITH2001-05-01 View
↑