ChoiceSpine Receives FDA Clearance for Blackhawk Interbody Fusion Device

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


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Julie Vetalice is ORTHOWORLD's Editorial Assistant. She has covered the orthopedic industry for over 20 years, having joined the company in 1999.

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