> ## Content Index
> Fetch the complete content index at: https://www.fdaweb.com/llms.txt
> Use this file to discover other available public pages before exploring further.

# NovaBone Putty Cleared for Intervertebral Disc Repair
- URL: https://www.fdaweb.com/novabone-putty-cleared-for-intervertebral-disc-repair/
- Published: 2024-11-13T12:00:00.000Z
- Updated: 2026-09-14T14:46:57.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5158180

FDA has cleared a NovaBone Products 510(k) for its bioactive synthetic bone graft, [NovaBone Putty,](https://novabone.com/orthopedics/products/novabone-putty?ref=fdaweb.com) and its expanded use in the intervertebral disc space. The clearance covers the device’s use in the intervertebral disc space alongside FDA-cleared interbody fusion devices, NovaBone says.

The company says the device has bioactive and osteostimulative properties, and it offers a “unique formulation of calcium sodium phosphosilicate (Bioglass) particulate mixed with a synthetic binder. The composition facilitates bone void filling and is gradually replaced by new bone tissue during the natural healing process.”