ChoiceSpine Receives FDA Clearance for Blackhawk Interbody Fusion Device

By Julie A. Vetalice

ChoiceSpine received FDA 510(k) clearance to market the Blackhawk™ anterior cervical fusion device.

Blackhawk, shown below, features self-locking anchors and a large center graft chamber. The anchors are designed to compress graft while leaving no profile outside of the interbody space.

Source: ChoiceSpine LP

Image courtesy of ChoiceSpine LP


Product Labels: Spinal Fusion

Tags: 510(k) Clearance, Regulatory