HOTWIRE™ RF Guidewire
FDA 510(k) clearance K240900 · decided 2024-05-01
Clearance details
- K-number
- K240900
- Device name
- HOTWIRE™ RF Guidewire
- Applicant
- Atraverse Medical
- Decision
- Substantially Equivalent
- Date received
- 2024-04-01
- Decision date
- 2024-05-01
- Days to decision
- 30 days
- Clearance type
- Traditional
- Product code
- DXF
- Device class
- 2
- Regulation number
- 870.5175
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Cardiff By The Sea, CA, US
- Third-party review
- Yes
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Atraverse Medical
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
Recalls involving this device
No recalls on record reference this clearance.