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

Atraverse Medical, Inc.

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

Total Devices2
Categories2
Latest Approval2025-08-27
TypeNumberDevice NameCodeDate
510(k) K252419 HOTWIRE RF GUIDEWIRE (901XXX); HOTWIRE RF GUIDEWIRE (902XXX) DXF 2025-08-27 View
510(k) K252083 HOTWIRE™ System RF Generator and Footswitch (optional accessory) GEI 2025-08-12 View