510(k) K051443
K051443 is an FDA 510(k) premarket notification submitted by Curasan Ag, Frankfurt Facility for the device "CERASORB DENTAL, CERASORB M DENTAL AND CERASORB PERIO". The FDA issued a decision of Substantially Equivalent on Jul 22, 2005. The device falls under product code LYC (Bone Grafting Material, Synthetic), a Class II device regulated under 21 CFR 872.3930.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jul 22, 2005
- Date Received
- Jun 2, 2005
- Clearance Type
- Abbreviated
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Bone Grafting Material, Synthetic
- Device Class
- Class II
- Regulation Number
- 872.3930
- Review Panel
- DE
- Submission Type
- 510(k)
A synthetic bone grafting material is synthetically-derived device, such as hydroxylapatite, intended to fill, augment, or reconstruct periodontal and or bony defects of the upper or lower jaw.