# K120152: Cerasorb Plus

- Pathway: 510(k) (Abbreviated)
- Applicant: Riemser Arzneimittel AG
- Decided: Aug 13, 2012 after 208 days
- Product code: NPM (Bone Grafting Material, Animal Source)
- Device class: 2
- Regulation: 21 CFR 872.3930
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K941780 (1995). 18 ancestors in all.
No later device cites it as a predicate yet.
0 of 19 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K051443: Cerasorb Dental, Cerasorb M Dental and Cerasorb Perio, Curasan Ag, Frankfurt Facility (2005) Summary page 1.

## Indications for use
CERASORB® Plus is recommended for: Defects after extirpation of bone cysts Augmentation of the atrophied jaw ridge Sinus lift or sinus base elevation respectively Filling alveolar defects after tooth extraction for jaw ridge support Filling extraction defects to create an implant site Filling of two or multi-walled infrabony pockets, and bifurcation and triflurcation defects Defects after operative removal of retained teeth or corrective osteotomes

Source page: https://510kreport.com/device/K120152
Methodology: https://510kreport.com/methodology