FDA grants Centinel Spine allogeneic bone graft indications for lumbar spinal fusion line — 5 key notes

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.

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