Denali™ Vena Cava Filter System – Femoral and Jugular/Subclavian Delivery Kit
FDA 510(k) clearance K240257 · decided 2024-02-29
Clearance details
- K-number
- K240257
- Device name
- Denali™ Vena Cava Filter System – Femoral and Jugular/Subclavian Delivery Kit
- Applicant
- Bd
- Decision
- Substantially Equivalent
- Date received
- 2024-01-31
- Decision date
- 2024-02-29
- Days to decision
- 29 days
- Clearance type
- Special
- Product code
- DTK
- Device class
- 2
- Regulation number
- 870.3375
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Tempe, AL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.