FDAnews Device Daily Bulletin
Medical Devices / Submissions and Approvals

Synergy’s BioSphere Putty Secures Regulatory Clearance in Australia

March 7, 2018
A A

Synergy Biomedical received clearance from Australia’s Therapeutic Goods Administration for its bioactive bone graft product BioSphere Putty.

The product uses spherical bioactive glass particles to create a moldable bone graft putty that improves bone formation.

The product previously received FDA and CE Mark clearances, and has been on the market since 2013.

View today's stories