By Laura Dyrda
Centinel Spine received an allogeneic bone graft indication for its anterior lumbar product family.
Here are five things to know:
1. The FDA cleared the STALIF MIDLINE, MIDLINE II and MIDLINE II-Ti (Ti-ACTIVE) devices for use with allogeneic bone graft in lumbar spinal fusions.
2. The Centinel Spine standalone devices have a no-profile design and are integrated interbody systems for use with autograft and/or allogeneic bone graft in lumbar and cervical fusion procedures.