# K033110: C-Graft

- Pathway: 510(k) (Traditional)
- Applicant: The Clinician'S Preference, LLC
- Decided: Dec 10, 2003 after 71 days
- Product code: LYC (Bone Grafting Material, Synthetic)
- 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: 2 generations back to K950165 (1995). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K023799: Frios Algipore, Friadent GmbH (2003) Summary page 1.
- K950165: Interpore IP 200 Granular Coralline Hydroxyapatite Bone Void Fillers, 425 to 1000 Microns and 425 to 600 Microns, Interpore Intl. (1995) Summary page 1.
- K981214: Osteograf/N-700, Ceramed Dental, LLC (1998) Summary page 1.

## Indications for use
C-GRAFTTM is indicated for: Augmentation of bony defects of the alveolar ridge Sinus elevation grafting Treatment of intrabony periodontal defects Extraction socket grafting

Source page: https://510kreport.com/device/K033110
Methodology: https://510kreport.com/methodology