510(k) K232955
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 10, 2024
- Date Received
- September 21, 2023
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Device, Neurovascular Embolization
- Device Class
- Class II
- Regulation Number
- 882.5950
- Review Panel
- NE
- Submission Type