510(k) K171451
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 8, 2017
- Date Received
- May 17, 2017
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Implant, Eye Valve
- Device Class
- Class II
- Regulation Number
- 886.3920
- Review Panel
- OP
- Submission Type