# K960353: Osteograf/LD-300 Hydroxylapatite

- Pathway: 510(k) (Traditional)
- Applicant: Ceramed Corp.
- Decided: Apr 18, 1996 after 84 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
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) OsteoGraf/D-700 (previously OsteoGraf/AR): named in the summary without a submission number

## Most influential descendants
- K072057: Osteograf/LD-300 (2007), 0 descendants of its own

## Indications for use
The intended use of OsteoGraf/LD-300 is for the filling of periodontal defects and augmentation of bony defects of the alveolar ridge, including tooth extraction sites.

Source page: https://510kreport.com/device/K960353
Methodology: https://510kreport.com/methodology