Atraverse Medical, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K260292HOTWIRE RF GUIDEWIRE (901XXX); HOTWIRE RF GUIDEWIRE (902XXX)February 27, 2026
K252419HOTWIRE RF GUIDEWIRE (901XXX); HOTWIRE RF GUIDEWIRE (902XXX)August 27, 2025
K252083HOTWIRE™ System RF Generator and Footswitch (optional accessory)August 12, 2025
K240900HOTWIRE™ RF GuidewireMay 1, 2024