510(k) K161166
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 8, 2016
- Date Received
- April 26, 2016
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Bone Cement, Antibiotic
- Device Class
- Class II
- Regulation Number
- 888.3027
- Review Panel
- OR
- Submission Type