510(k) K093231
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 14, 2010
- Date Received
- October 14, 2009
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Graft, Vascular, Synthetic/Biologic Composite
- Device Class
- Class II
- Regulation Number
- 870.3450
- Review Panel
- CV
- Submission Type